Safety Recalls

17,559 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 2,601–2,650 of 17,559

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026

  Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

  Class I

• Medical Device Recall · April 10, 2026

  Medline Industries, LP

  Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B;

  Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.

  Class I

• Medical Device Recall · April 10, 2026

  Stryker Sustainability Solutions

  Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER

  Incomplete seals on sterile product

  Class II

• Medical Device Recall · April 10, 2026

  ARROW INTERNATIONAL, LLC

  Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-I

  16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.

  Class I

• Consumer Product Recall · April 9, 2026

  BISSELL Homecare Inc. of Grand Rapids, Michigan

  Steam Shot OmniReach and Steam Shot Omni Steam Cleaners with attachments

  The recalled steam cleaners' attachments can unexpectedly detach from the steam cleaners and expel hot water or steam onto users during use, posing a serious burn hazard.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Zhongshan Yungu Daily Products, of China

  Easymake Adult Portable Bed Rails

  The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Prestige Import Group, of Deerfield, Florida

  Supernova and Typhoon Lighters

  The recalled lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanism, posing a risk of serious injury or death from fire and burn hazards. In addition, the lighters failed to meet the pre-market lighter submission requirement needed to demonstrate that the lighters feature child-resistant mechanisms and ensuring their safety and compliance with U.S. regulations.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Snooz, Inc., of Las Vegas, Nevada

  Breez 2-in-1 Smart Bedroom Fan and White Noise Machine

  The power connector inside the fan can corrode and cause the fan to overheat, posing a risk of fire.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Weifang Luzhan Trade Co., Ltd., dba Yeeluzan, of China

  Yeeluzan Pool Drain Covers

  The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.

  Unclassified

• Medical Device Recall · April 9, 2026

  Stryker Corporation

  Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the FluidSmart Fluid Management System, which is intended for irri

  Due to nonconforming products being inadvertently distributed.

  Class II

• Vehicle Recall · April 9, 2026

  Chrysler (FCA US, LLC)

  2025 RAM 5500, 2025 RAM 3500, 2026 RAM 3500

  An instrument panel display that fails to show critical safety information, such as gear selection and warning lights, increases the risk of a crash.

  Unclassified

• Drug Recall · April 9, 2026

  The Harvard Drug Group LLC

  Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister cards) per carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46288. NDC: 0

  Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.

  Class II

• Consumer Product Recall · April 9, 2026

  ShymeryDirect, of China

  ShymeryDirect LED Lights

  The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. If coin batteries are swallowed, they can cause serious injuries, internal chemical burns and death.

  Unclassified

• Consumer Product Recall · April 9, 2026

  LinkInnow International Co., Ltd., dba Besslly Store, of China

  Besslly Halloween Pumpkin Carving Kits

  The recalled carving kits violate the mandatory standard for consumer products with button cell and coin batteries because the button cell batteries in the tea lights can be accessed easily by children, posing an ingestion hazard. Additionally, the product and its packaging do not have the warnings required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Head USA Inc., of Boulder, Colorado

  Head Ski Boots

  The fluorescent yellow materials of the boot shell and sole inserts can deteriorate and break, posing a risk of serious injury from a fall.

  Unclassified

• Consumer Product Recall · April 9, 2026

  J U Kai Technology Co., LTD, dba Happiness Light, of China

  Happiness Light LED Lights

  The recalled LED lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain lithium coin batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Hefei Maitusilu Wangluokeji Youxiangongsi, dba Maitys, of China

  Maitys Drinkware Charms

  The recalled magnetic drinkware charms violate the mandatory standard for magnets because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Qingyuan Fenle Sauna & Pool Equipment Co., Ltd., of China

  Muscccm Pool Drain Covers

  The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Johnson Outdoors Diving LLC d/b/a SCUBAPRO, of Racine, Wisconsin

  SCUBAPRO Monorail Weight Pockets for BCDs

  The D-ring handle that is used to unlock the weight pocket from the Buoyancy Compensator Device (BCD) can detach during use. If this happens, the user will not be able to remove the weight pocket in an emergency, in order to rise to the surface, posing a risk of serious injury or death from a drowning hazard.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Shenzhen Baihang Technology Co., Ltd., of China

  VEEKTOMX Portable Charger Mini Power Banks

  The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Shenzhen Shijingjie Network Technology Co., Ltd., of China

  Male-to-Male Extension Cords

  The recalled male-to-male extension cords violate safety requirements because their exposed prongs can become energized when one end is plugged into a generator or other power source, posing a risk of serious injury and death from electrocution. In addition, using the cords to supply power from a generator to a residential electrical system (backfeeding) poses a risk of electrocution and fire. The cords' short length encourages the use of generators close to homes or enclosed spaces, posing a risk of carbon monoxide (CO) poisoning.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Wybotics, Co. Ltd. of Tianjin, Chin

  Osprey 700 Max and S1 robotic pool vacuums

  The lithium-ion battery in the recalled pool vacuums can overheat, posing burn and fire hazards to consumers.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Vitaquest International LLC of West Caldwell, New Jersey

  Various Brands of Iron-Containing Dietary Supplements

  The dietary supplements contain iron, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The packaging of the supplements is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Seasonal Specialties, LLC, of Eden Prairie, Minnesota

  Members Mark 7' Pre-Lit Twinkling Buck

  If the wires are connected incorrectly, the current limiting resistor can overheat, posing a burn hazard.

  Unclassified

• Consumer Product Recall · April 9, 2026

  Silks, of Queen Creak, Arizona

  Children's Loungewear Sets

  The recalled children's loungewear violates mandatory flammability standards for children's sleepwear, posing a risk of serious injuries or deadly burn hazards to children.

  Unclassified

• Drug Recall · April 8, 2026

  Blaine Labs Inc

  TERPENICOL Antifungal Solution, (Undecylenic (10-Undecenoic) acid 25%), 1.0 Fl Oz (29.6 mL), Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Santa Fe Springs, CA 90670. NDC 63347-600-01

  CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

  Class II

• Drug Recall · April 8, 2026

  Apotex Corp.

  Desmopressin Nasal Spray, USP, 10 mcg/0.1 mL, 5 mL bottle (50 doses), Rx only, Mfg by: Apotek inc., Toronto, Ontario, Canada, M9L 1T9, Mfg for: Apotek Corp., Weston, FL 33326, NDC 60505-0815-0

  Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.

  Class II

• Food Recall · April 8, 2026

  Pure Ground Ingredients, Inc.

  Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk; tea/food manufacturers. Closed container stored in a cool settings at ambient/room temperature, free of direct sunlight. Packagi

  Product has the potential to be contaminated with Salmonella.

  Class I

• Medical Device Recall · April 8, 2026

  Hologic, Inc

  3DIMENSIONS MAMMOGRAPHY SYSTEM; Model Numbers: 3DM-SYS-INTL2D, 3DM-SYS-INTL2D-MOB, 3DM-SYS-INTL2D-NS, 3DM-SYS-INTL3D, 3DM-SYS-INTL3D-MOB, 3DM-SYS-INTL3D-NS, 3DM-SYS-STD, 3DM-SYS-STD-MOB, 3DM-SYS-STD-N

  Complaints have been received of systems developing loose, missing, or broken internal bolts over time.

  Class II

• Medical Device Recall · April 8, 2026

  Hologic, Inc

  SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6000-3D, SDM-00001-2D, SDM-00001-3D, SDM-00001-M2D, SDM-00001-M3D, SDM-05000-2A2,

  Complaints have been received of systems developing loose, missing, or broken internal bolts over time.

  Class II

• Drug Recall · April 8, 2026

  Blaine Labs Inc

  TRIFLUENT PHARMA TRIDERGEL Wound Care Gel, (Benzalkonium Chloride 0.1%), 1.0 fl oz, (29.6 mL) bottle with long pointy cap, Manufactured for: Trifluent Pharma, LLC. San Antonio, TX 78213. NDC 73352-520

  CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated

  Class II

• Medical Device Recall · April 8, 2026

  Becton, Dickinson and Company

  Swan-Ganz Pacing Catheter, Models: D200F7;

  Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

  Class II

• Drug Recall · April 8, 2026

  Blaine Labs Inc

  Fungal Fusion ERADICATION Solution, Antifungal & Antimicrobial Kit. Contains, 1x2 oz bottle Fungal Fusion Antifungal (Miconazole Nitrate) Cream, 1x2oz bottle Fungal Fusion Antifungal Solution (25% Un

  CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

  Class II

• Medical Device Recall · April 8, 2026

  Becton, Dickinson and Company

  Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 831F75/831F75P, TS105F5, 774F75, 777F8, AIQSGF8;

  Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

  Class II

• Drug Recall · April 8, 2026

  Blaine Labs Inc

  TERPENICOL Antifungal Cream (Undecylenic Acid 13%), 1.0 oz (28 g) bottles, Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Sante Fe Springs, CA 90670, NDC 63347-601-01.

  CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

  Class II

• Medical Device Recall · April 8, 2026

  Becton, Dickinson and Company

  Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P

  Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

  Class II

• Drug Recall · April 8, 2026

  Blaine Labs Inc

  Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37 mL) bottle, shorter twist cap, Manufactured By: Blaine Labs, Inc. 11037 Lockport Place Santa Fe Springs, CA 90670, NDC

  Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp

  Class I

• Drug Recall · April 8, 2026

  Blaine Labs Inc

  Revitaderm Wound Care, First Aid Antiseptic Gel, Benzalkonium Chloride 0.1%) packaged as (a) 1.0 Fl OZ (16 mL) bottle, long pointy cap, NDC 63347-120-02; (b) 3.0 Fl OZ (85 g) tube, with short twist ca

  CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated

  Class II

• Drug Recall · April 8, 2026

  Blaine Labs Inc

  TRIPENICOL S Antifungal Solution (Undecylenic Acid 25%), 1.25 FL OZ (37.5 mL) bottle, Manufactured For: Trifluent Pharma, LLC, San Antonio, TX 78213, NDC 73352-550-01.

  CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

  Class II

• Drug Recall · April 8, 2026

  Blaine Labs Inc

  vite20 Antifungal Cream, (10% Undecylenic Acid), 0.54 OZ (15 g) bottle, Manufactured By: Blaine Labs, Inc., 11037 Lockport Place, Sante Fe Springs, CA 90670, UPC 6 16728 00039 2.

  CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry

  Class II

• Medical Device Recall · April 8, 2026

  Medtronic Neuromodulation

  Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900A CLINICIAN TABLET US, Model Number CT900A; 2. PROG CT900B

  Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest. However, in rare cases, the steps may be displayed out of order. If this occurs, the programmed Flex Infusion schedule will not be delivered at the intended time, if at all.

  Class II

• Drug Recall · April 7, 2026

  Water-Jel Technologies, LLC

  Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950

  Failed PH Specifications

  Class III

• Medical Device Recall · April 7, 2026

  Becton Dickinson & Co.

  BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use

  BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.

  Class II

• Food Recall · April 7, 2026

  Marquez Brothers International, Inc.

  EL MEXICANO horchata casera Instant Horchata Drink NET WT 14oz (396g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95138 UPC

  Undeclared milk.

  Class II

• Medical Device Recall · April 7, 2026

  Becton Dickinson & Co.

  BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use

  BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.

  Class II

• Drug Recall · April 7, 2026

  Hikma Pharmaceuticals USA INC

  Alendronate Sodium Oral Solution, 70 mg/75 mL, 75 mL, Rx only, 4 x 75 mL Single Dose Bottles, Distr. by: Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ 07922, NDC 0054-0282-59.

  This recall is being conducted due to out of specification assay results in a limited number of bottles that were stored on side.

  Class II

• Food Recall · April 7, 2026

  Marquez Brothers International, Inc.

  Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547

  Undeclared milk.

  Class II

• Food Recall · April 7, 2026

  Marquez Brothers International, Inc.

  EL MEXICANO agua fresca de horchata Instant Horchata Drink NET WT 12oz (340g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95

  Undeclared milk.

  Class II

• Food Recall · April 6, 2026

  LIQUID BLENZ CORP

  Pure Shilajit Tonic 16 oz and 32 oz

  May be under-processed resulting in growth of Clostridium botulinum and lists health claims.

  Class II