Safety Recalls

15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 7,801–7,850 of 15,271

• Drug Recall · February 20, 2025

  Central Admixture Pharmacy Services, Inc.

  PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, 855-275-2270, NDC 7

  Presence of Particulate Matter

  Class I

• Consumer Product Recall · February 20, 2025

  Dongguanshi Yanxiang Keji Youxiangongsi, dba SEJOV, of China

  SEJOV Five-Drawer Dressers

  The recalled dressers are unstable if they are not properly anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate performance and warning label requirements of the STURDY Act.

  Unclassified

• Drug Recall · February 20, 2025

  One Source Nutrition, Inc,

  Vitality, Fast Acting Male Enhancement Product, Dietary Supplement, a) One Capsule per Packet, b) 6 capsules per bottle, Xtreme Potency.

  Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared sildenafil and tadalafil.

  Class I

• Consumer Product Recall · February 20, 2025

  Kubota Tractor Corporation, of Grapevine, Texas

  Kubota Utility Tractors model MX5400DTC

  The clutch cable can break on the recalled MX5400DTC utility tractors, resulting in reduced braking power, posing a crash hazard.

  Unclassified

• Consumer Product Recall · February 20, 2025

  OdorStop LLC, of Hamburg, New York

  OdorStop Boot and Shoe Dryers and Deodorizers

  The heat or ozone on-off switch can short circuit, resulting in arcing, posing a fire hazard.

  Unclassified

• Medical Device Recall · February 20, 2025

  Microbiologics Inc

  Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus (Pellet), Multi-analyte, unassayed quality control material, Catalog Number HE0065N

  The A549 human cell target (human cells for sample adequacy control) may give a late Ct value.

  Class II

• Consumer Product Recall · February 20, 2025

  Shadeks LLC, of Bensalem, Pennsylvania

  ShadesU Roller Window Shades

  The recalled window blinds have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window blinds are in violation of the federal regulations for window coverings and present a substantial product hazard. The window blinds also violate federal regulations for labeling of window coverings.

  Unclassified

• Consumer Product Recall · February 20, 2025

  Swagtron, of South Bend, Indiana

  Swagtron SG-5 Swagger 5 Boost Commuter Electric Scooters

  The electric scooters' lithium-ion batteries can overheat, smoke, melt and ignite, posing fire and burn hazards, posing a risk of serious injury and death.

  Unclassified

• Consumer Product Recall · February 20, 2025

  Zhejiang Mingjing Textile Co. Ltd, of China

  Homebox Blackout Roller Window Shades

  The recalled window blinds have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The window blinds are in violation of the federal regulations for window coverings and present a substantial product hazard. The window blinds also violate federal regulations for labeling of window coverings.

  Unclassified

• Consumer Product Recall · February 20, 2025

  SuperATV, of Madison, Indiana

  SuperATV carrier bearings for Polaris RZR XP Turbo or Turbo S Recreational Off Highway Vehicles (ROVs)

  When the recalled carrier bearings are installed in a Polaris RZR XP Turbo or Turbo S vehicle and the fuel tank expands, the drive shaft can come in contact with the fuel tank, causing the tank to develop a hole or crack. This can cause the fuel tank to leak gasoline, posing fire and burn hazards.

  Unclassified

• Medical Device Recall · February 20, 2025

  BD SWITZERLAND SARL

  BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and hemodynamic pressu

  Due to specific lots of luer-lok devices were shipped to the U.S. market with an Outside US Instruction for Use (IFU)

  Class II

• Consumer Product Recall · February 20, 2025

  Fjorden Electra AS, of Norway

  Fjorden iPhone Camera Grips

  The recalled camera grips violate the mandatory federal regulation for consumer products containing button cell and coin batteries because, when the product is dropped, the battery tray can separate from its compartment, making the lithium coin battery easily accessible by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

  Unclassified

• Consumer Product Recall · February 20, 2025

  DR Power Equipment, of South Burlington, Vermont, a subsidiary of Generac Power Systems Inc., of Waukesha, Wisconsin

  Tow Behind Field and Brush Mowers

  The blade carrier spindle bolt can become loose, causing the blade assembly to detach while the mower is in operation, posing a laceration hazard to the user.

  Unclassified

• Consumer Product Recall · February 20, 2025

  Holosun Technologies Inc., of City of Industry, California

  Holosun Firearm Dot Sights

  The recalled Holosun Red and Gold Firearm Dot Sights violate the mandatory federal regulations for consumer products containing button cell or coin batteries because the lithium coin battery can be easily accessed, posing an ingestion hazard. The products include a lithium coin battery which is not in child-resistant packaging, as required by Reese's Law. In addition, the products do not bear the required warnings. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

  Unclassified

• Consumer Product Recall · February 20, 2025

  Nazzaro Enterprises Texas Inc., of Hurst, Texas

  Rebecca's Toys & Prizes Bowling Pin Sipper Cups

  The red tape on the bowling pin sipper cups contains levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.

  Unclassified

• Consumer Product Recall · February 20, 2025

  Sauder Woodworking Co., of Archbold, Ohio

  Sauder and Sauder Beginnings Dressers and 4-Drawer Chests tip-over restraint straps

  The tip-over restraint straps can fail when used on certain Sauder clothing storage units (dressers and 4-drawer chests) to prevent tip-over incidents, posing tip-over and entrapment hazards that can result in death or serious injuries to children.

  Unclassified

• Consumer Product Recall · February 20, 2025

  Triumph Motorcycles America Ltd., of Atlanta, Georgia

  Triumph TF250-X Closed Course Competition Motorcycles

  The right-hand plastic switch cube can crack when exposed to brake fluid, causing a short circuit that starts the motorcycle unexpectedly, posing an injury hazard.

  Unclassified

• Consumer Product Recall · February 20, 2025

  Super73 Inc., of Irvine, California

  Model Year 2024 Z Miami SE and Z Adventure Core Electric Bicycles

  The retaining pin in the e-bike's disc brake calipers can loosen and dislodge from the caliper assembly, resulting in brake failure, posing crash and injury hazards to the rider.

  Unclassified

• Consumer Product Recall · February 20, 2025

  Trek Bicycle Corporation, of Waterloo, Wisconsin

  Electra E-bikes

  The rear fender can come loose and can contact the rear wheel and stop the bike unexpectedly, causing the rider to lose control of the bike, posing a crash hazard.

  Unclassified

• Medical Device Recall · February 19, 2025

  GE Healthcare

  GE Healthcare Centricity Cardiology CA1000 (CA1000), Model Numbers: 1) 2033901-001; 2) 2038437-001; 3) 2038437-009; 4) 2038437-014; 5) 2038437-015 ; 6) 2038437-0XX; 7) 2109571-007; 8)

  There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

  Class II

• Medical Device Recall · February 19, 2025

  Merge Healthcare, Inc.

  VERICIS, Merge Cardio, Model/Catalog Number: Version 9.x, Software Version: 9.0.6 and 9.0.8; VERICIS is an integrated cardiovascular information system classified as a picture archiving and communica

  When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

  Class II

• Medical Device Recall · February 19, 2025

  GE Healthcare

  GE Healthcare Centricity Universal Viewer (UV), Model Numbers: 1) 2066908-077; 2) 2066908-136; 3) 2066908-150; 4) 2088026-003; 5) 2088026-026; 6) 2088026-032; 7) 2088026-043; 8) 2088026-

  There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

  Class II

• Medical Device Recall · February 19, 2025

  Merge Healthcare, Inc.

  VERICIS, Merge Cardio, Model/Catalog Number: Version 11.x, Software Version: 11.0.2, 11.0.3, 11.0.4, 11.1, 11.1.1; The VERICIS is an integrated cardiovascular information system classified as a pictur

  When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

  Class II

• Medical Device Recall · February 19, 2025

  GE Healthcare

  GE Healthcare Centricity PACS-IW (PACS-IW), Model Numbers: 1) 2042988-001; 2) 2049587-009; 3) 2049587-011; 4) 2049587-012; 5) 2049587-015; 6) 2049588-012 ; 7) 2052829-001.

  There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

  Class II

• Medical Device Recall · February 19, 2025

  GE Healthcare

  GE Healthcare Centricity Radiology RA600 (RA600), Model Numbers: 1) 2022296-001; 2) 2033901-001; 3) 2038437-001; 4) 2038437-011; 5) 2038437-012; 6) 2038437-013; 7) 2038437-014; 8) 203

  There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

  Class II

• Medical Device Recall · February 19, 2025

  Flux Technology Inc.

  Lazervida 10W diode laser cutter and engraver with Lazervida shield.

  Lazervida 10W Diode Laser Engraver does not fully meet current Federal performance standards in certain areas. Specifically, the product does not incorporate the additional beam attenuator, remote interlock connector, key switch, specific labels and manual instructions required under current regulations.

  Class II

• Medical Device Recall · February 19, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT, Model Number: MJ18004V2; 2) MJ BANDAGE HYDROCOLLOID ALL PURP 10CT, Model Number: MJ18005V2; 3) MJ BNDG HYDROCOLLOID FINGER TO

  There is a potential for the sterility of the device to be compromised.

  Class II

• Food Recall · February 19, 2025

  Elwood International, Inc.

  Calais Brand Grape jelly; 128 FL. OZ. (1 GAL.) 3.785 L; INGREDIENTS: Grape Juice, Corn Syrup, High Fructose Corn Syrup, Pectin, Citric Acid; REFRIGERATE AFTER OPENING; UPC 040264 10128 0

  Contains undeclared colors (FD&C Blue 1 and FD&C Red 40)

  Class III

• Medical Device Recall · February 19, 2025

  MEDLINE INDUSTRIES, LP - Northfield

  Wayson Hydrocolloid Models: 1) Model Number: CUR5103, DBD-BNDG,WTRPRF,HYDRCLLD,CLR,2.36X3.93", 2) Model Number: MJ18004, DBD-MEIJER,BANDAGE,HYDROCOLLOID,HEEL,OVL 3) Model Number: MJ18005, MEIJER,BA

  There is a potential for the sterility of the device to be compromised.

  Class II

• Medical Device Recall · February 19, 2025

  Calyxo, Inc.

  CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of urinary tract and kidney interior.

  Aspiration system, for endoscopic examination/treatment of urinary tract and kidney interior, to have labeling update adding additional instructions, for patients with high viscosity fluid in the kidney, not to continue providing fluid inflow in the presence of unresolved slow or absent fluid outflow because this can create intrarenal pressure imbalance, and lead to excessive intrarenal pressure.

  Class I

• Medical Device Recall · February 19, 2025

  GE Healthcare

  GE Healthcare Centricity Centricity PACS-IW with Universal Viewer, Model Numbers: 1) 2049587-015; 2) 2066908-086; 3) 2066908-136; 4) 2104867-045.

  There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.

  Class II

• Medical Device Recall · February 19, 2025

  Merge Healthcare, Inc.

  VERICIS, Merge Cardio, Model/Catalog Number: Version 10.x, Software Version: 10.0, 10.1.1.1, 10.1.2, 10.2.0, 10.2 P2 , 10.3; The VERICIS is an integrated cardiovascular information system classified a

  When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

  Class II

• Medical Device Recall · February 19, 2025

  Merge Healthcare, Inc.

  Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.1, 12.1.1, 12.2, 12.3, 12.3.1, 12.3.2, 12.3.3, 12.4, 12.4.1, 12.4.2; Merge Cardio is a software medical device that is an integra

  When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

  Class II

• Medical Device Recall · February 19, 2025

  Merge Healthcare, Inc.

  VERICIS, Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.0.1, 12.0.2; The VERICIS is an integrated cardiovascular information system classified as a picture archiving and commun

  When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.

  Class II

• Medical Device Recall · February 19, 2025

  MIM Software Inc

  MIM software; System, Image Processing, Radiological

  In situations where two images with differing Fields of View (FOV) complete an image fusion, an incorrect, elevated Maximum Standardized Uptake Value (SUV) within MIM Software versions 7.2.0 through 7.2.6.could result.

  Class II

• Food Recall · February 18, 2025

  AKT Trading Inc.

  Choshiya branded "RAKKYO ZUKE PREPARED VEGETABLES" UPC# JANCODE 4983673526021

  Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.

  Class I

• Medical Device Recall · February 18, 2025

  GE Medical Systems, LLC

  GE Healthcare Revolution Apex Elite, System, X-ray, Tomography, Computed

  GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.

  Class II

• Drug Recall · February 18, 2025

  Turbare Manufacturing

  Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not for Resale - Single Use, This drug product was repackaged by Turbare Manufacturing, 925 Jeanette Driv

  Lack of Assurance of Sterility: due to a quality control process deviation

  Class II

• Food Recall · February 18, 2025

  Growland Inc

  Dried Longan Pulp- Made in China, 8oz(227g), GROWLAND INC. rear panel- Organic Planted, Store in cool and dry place, Made in Thailand; UPC# 8 513041 327262

  Elevated levels of Sulfites in Dried Longan Pulp

  Class II

• Food Recall · February 18, 2025

  AKT Trading Inc.

  Choshiya branded "FUKUSHIN ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535142

  Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.

  Class I

• Food Recall · February 18, 2025

  AKT Trading Inc.

  Choshiya branded "AOKAPPA ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535135

  Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.

  Class I

• Medical Device Recall · February 18, 2025

  CareFusion 303, Inc.

  BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management Software

  Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).

  Class I

• Food Recall · February 18, 2025

  AKT Trading Inc.

  Choshiya branded "SHIBA ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535128

  Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.

  Class I

• Food Recall · February 18, 2025

  AKT Trading Inc.

  Choshiya branded "SOFT TSUBOZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535159

  Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.

  Class I

• Medical Device Recall · February 18, 2025

  GE Medical Systems, LLC

  GE Healthcare Revolution Apex Expert, System, X-ray, Tomography, Computed

  GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.

  Class II

• Medical Device Recall · February 18, 2025

  GE Medical Systems, LLC

  GE Healthcare Revolution Apex Plus, System, X-ray, Tomography, Computed

  GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.

  Class II

• Medical Device Recall · February 18, 2025

  CareFusion 303, Inc.

  BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software

  Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).

  Class I

• Food Recall · February 18, 2025

  AKT Trading Inc.

  Choshiya branded "MENMA AJITSUKE PREPARED BAMBOO SHOOTS" UPC# JANCODE 4983673527325

  Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.

  Class I

• Medical Device Recall · February 18, 2025

  GE Medical Systems, LLC

  GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed

  GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.

  Class II

• Medical Device Recall · February 18, 2025

  GE Medical Systems, LLC

  GE Healthcare Revolution Apex Select, System, X-ray, Tomography, Computed

  GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.

  Class II