Safety Recalls

17,553 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 1,801–1,850 of 17,553

• Food Recall · May 12, 2026

  Straus Family Creamery

  STRAUS FAMILY CREAMERY Vanilla Bean ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100306

  Potential contamination with foreign objects (metal pieces).

  Class II

• Food Recall · May 12, 2026

  Straus Family Creamery

  STRAUS FAMILY CREAMERY Dutch Chocolate ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100122

  Potential contamination with foreign objects (metal pieces).

  Class II

• Food Recall · May 11, 2026

  HH FRESH TRADING CORP

  HH Fresh Trading Corp. (branded) ENOKI MUSHROOM; Premium Quality; Net WT/ Poids Net 150g(5.29oz) Distributed by HH Fresh Trading Exported by JIA YANG INTERNATIONAL ENTERPRISES CO., LTD. Produced by Gr

  Imported Enoki Mushrooms tested positive for Listeria Monocytogenes.

  Class I

• Vehicle Recall · May 11, 2026

  Braun Corporation

  2023 CHRYSLER PACIFICA, 2024 CHRYSLER PACIFICA, 2025 CHRYSLER PACIFICA

  An unsecured wheelchair can move during transit, increasing the risk of injury.

  Unclassified

• Medical Device Recall · May 11, 2026

  Zimmer, Inc.

  Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description: Persona Revisi

  Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.

  Class II

• Medical Device Recall · May 11, 2026

  Inspire Medical Systems Inc.

  Brand Name: Inspire Medical Systems, Inc. Product Name: Inspire Respiratory Sensing Lead Model/Catalog Number: 4340 Software Version: N/A Product Description: The Inspire¿ Respiratory Sensing Lead

  Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By Date may result in unplanned or premature revision surgery.

  Class II

• Medical Device Recall · May 11, 2026

  Fresenius Medical Care Holdings, Inc.

  5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush Standard Blood Tubing Set; Model Number: 03-5110-6. 2. 5008X HD/HDF Standard B

  Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem.

  Class II

• Medical Device Recall · May 11, 2026

  Boston Scientific Corporation

  Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device

  There is the potential for leakage along the drug pathway from the pump through the end of the catheter.

  Class II

• Medical Device Recall · May 11, 2026

  Inspire Medical Systems Inc.

  Brand Name: Inspire Medical Systems, Inc. Product Name: Inspire stimulation Lead Model/Catalog Number: 4063 Product Description: The Inspire¿ Stimulation Lead (Model 4063) is designed to deliver st

  Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a product past its Use By Date may result in unplanned or premature revision surgery.

  Class II

• Medical Device Recall · May 11, 2026

  Terex Utilities

  Power Over Fiber Base Module

  Device not certified - no laser product report was filed with CDRH prior to distribution. Product label incorrectly states device is "Class IV", although Class 1 is appropriate for device. Improperly labeled - omitted labels required under 21 CFR 1040.10 / IEC 60825-1 via LN#56. Missing certification and proper manufacturer's ID label. Was not accompanied by compliant User Information. Formalized quality control procedures and record keeping of QC testing was not performed to IEC 60825-1 nor 21 CFR 1040.10 standards. Sales information did not convey required class designation and warning statement

  Class II

• Drug Recall · May 11, 2026

  Haleon US Holdings LLC

  Gas-X, Simethicone 125 mg/ ANTIGAS, 120 SoftGels, Distributed by: Haleon, Warren, NJ 07059, UPC: 3 00674 35041 9.

  Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling.

  Class II

• Medical Device Recall · May 11, 2026

  In2bones USA, LLC

  NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic Compression Staple w/Instruments, Size 10x10x10 UDI-DI Code: 00817906020083

  Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.

  Class II

• Medical Device Recall · May 8, 2026

  Instrumentation Laboratory

  Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number: 00024019255 Portable blood analyzer system

  Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

  Class II

• Medical Device Recall · May 8, 2026

  Ventec Life Systems, Inc.

  VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001

  Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result in the backup alarm not activating during loss of primary power and absence/depletion of backup power sources, which may result in delayed caregiver awareness of a hazardous condition.

  Class II

• Medical Device Recall · May 8, 2026

  AMD Medicom Inc.

  Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in, Non-Sterile/55994C; 0.75x0.75in, Non-Sterile/55995C; 1.0x1.0in, Non-Ste

  Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

  Class II

• Medical Device Recall · May 8, 2026

  Think Surgical, Inc.

  TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instr

  Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.

  Class II

• Medical Device Recall · May 8, 2026

  Instrumentation Laboratory

  GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Portable blood analyzer system. Affected Accessory: Bar Code Read

  Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

  Class II

• Medical Device Recall · May 8, 2026

  Datex-Ohmeda Inc

  Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (resuscitator) Product identifiers: 2082663-001, 2082663-002, M1241424 Product impacted only if service blender M10916

  Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.

  Class I

• Medical Device Recall · May 8, 2026

  GE Medical Systems SCS

  GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System

  GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client worklist and launches an interactive application (e.g. Volume Viewer), the application may open the previous patient's exam instead of the intended one. When this issue occurs, there is no system warning or error notification. If the error is not recognized, a clinical user could review, interpret, or report images for the wrong patient which could lead to misdiagnosis, incorrect clinical decisions, resulting in delayed or incorrect treatment.

  Class II

• Medical Device Recall · May 8, 2026

  Datex-Ohmeda Inc

  Giraffe Warmer with Integrated Resuscitation System (iRes), Panda Warmer with Integrated Resuscitation System (iRes) Product Identifiers: M1118179, M1112198 Impacted only if service blender M1091607-

  Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.

  Class I

• Medical Device Recall · May 8, 2026

  Instrumentation Laboratory

  Brand Name: GEM Premier 7000 with iQM3 Product Name: GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Intelligent Quality Management 3 (iQM3) is used as the quality control (QC) and asses

  Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

  Class II

• Medical Device Recall · May 8, 2026

  Datex-Ohmeda Inc

  Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-001 Impacted only if service blender M1091607-R was installed during the last Preventative Maintenance.

  Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.

  Class I

• Food Recall · May 8, 2026

  J and J Bunting, Inc

  Lunds & Byerly's Curry Powder Sweet

  Sesame Seeds White were labeled as Curry Powder Sweet.

  Class II

• Medical Device Recall · May 8, 2026

  Instrumentation Laboratory

  Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number: 00024019255 portable blood analyzer system

  Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

  Class II

• Medical Device Recall · May 8, 2026

  AMD Medicom Inc.

  Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 85995C

  Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet endotoxin specification for devices that contact the cerebrospinal fluid. Elevated endotoxin levels may lead to neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

  Class II

• Medical Device Recall · May 8, 2026

  Merit Medical Systems, Inc.

  Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669 00884450529690 REF: MSWSTDA35180 UDI-DI codes: 00884450529645 00884450529669 REF: MSWSTDA

  Due to unsealed portions of pouches.

  Class II

• Medical Device Recall · May 8, 2026

  Instrumentation Laboratory

  Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number: 00024019255 portable blood analyzer system

  Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

  Class II

• Medical Device Recall · May 8, 2026

  Instrumentation Laboratory

  Brand Name: GEM Premier 5000 Product Name: GEM Premier 5000 Model/Catalog Number: 00024019255 Portable blood analyzer system

  Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

  Class II

• Drug Recall · May 8, 2026

  UCB Biosciences Inc.

  cimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrna, GA 30080, a) NDC 50474-710-79, b) Professional sample, NDC 50474-710-80; c) 3 ca

  Lack of Assurance of Sterility

  Class II

• Food Recall · May 8, 2026

  Fly By Jing Inc.

  Fly By Jing (branded) Creamy Sesame Noodles; 3.8 oz packets. Sold in single and 4 packs. Single UPC: 8-50052-23988-6 4 pack UPC: 8-50052-23991-6

  Possible cross-contamination resulting in undeclared allergen ingredient (Peanut)

  Class II

• Medical Device Recall · May 7, 2026

  Siemens Healthcare Diagnostics, Inc.

  Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay

  A potential positive bias in quality control (QC) and patient sample results in three lots of the Dimension Tacrolimus (TAC) Flex reagent cartridge.

  Class II

• Consumer Product Recall · May 7, 2026

  Shenzhen Jijia Trading Co., Ltd., dba Justforjoyful, of China

  Justforjoyful Rainbow Wall Toys

  The recalled toys violate the mandatory safety standard for children's toys because the drumstick that is attached to the xylophone component has a spherical end that can pose a choking hazard.

  Unclassified

• Medical Device Recall · May 7, 2026

  Draeger, Inc.

  Atlan A350. Model Number: 8211500. anesthesia workstation

  The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

  Class I

• Medical Device Recall · May 7, 2026

  Fresenius Medical Care Holdings, Inc.

  Bicarby Dialysate; Model number: RFP-400-G;

  There is an error in the labeling of the GTIN on the product. When scanned; however, the case labeling, lot number, and printed labeling on the product correctly identifies the product code and the solution contained in the bag. In the event the incorrect GTIN labeling is used as the singular source for product identification, unrecognized use of a potassium solution with a concentration differing from the prescription may result.

  Class II

• Medical Device Recall · May 7, 2026

  PIE Medical Imaging B.V.

  3mensio Workstation (Vascular Fenestrated) software

  User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to 34.4%) than the actual anatomical dimension, if all the following occur: affected software is used, and the user has access only to 3D Echo OR Mitral 3D Echo, and the dataset being analyzed is a Philips 3D echo dataset containing Color Doppler information

  Class II

• Consumer Product Recall · May 7, 2026

  Shenzhen Favoto Co., Ltd., doing business as Favoto, of China

  Favoto Bike Helmets

  The recalled helmets violate the mandatory safety standard for bicycle helmets because they do not comply with the positional stability, labeling and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

  Unclassified

• Consumer Product Recall · May 7, 2026

  New Earth Technologies d.o.o., dba Analemma, of Zagreb, Croatia

  Analemma Water Bottles

  The recalled water bottle's inner glass liner can break, posing a risk of serious injury or death from laceration and ingestion hazards.

  Unclassified

• Vehicle Recall · May 7, 2026

  Chrysler (FCA US, LLC)

  2023 JEEP CHEROKEE

  A failed PTU may result in a loss of drive power or vehicle rollaway, increasing the risk of a crash or injury.

  Unclassified

• Consumer Product Recall · May 7, 2026

  Natural Pigments LLC, of Willits, California

  Rublev Colours Gum Turpentine and Mineral Spirits Bottles

  The gum turpentine and mineral spirits contain turpentine and low-viscosity hydrocarbons, respectively, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The bottles are 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 · May 7, 2026

  ZMC Group, Inc., of Los Angeles, California

  Various Battery-operated Light Up Toys

  The recalled toys violate the mandatory safety standard for children's toys because the toy contains button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

  Unclassified

• Consumer Product Recall · May 7, 2026

  shenzhenkaiwendishangmaoyouxiangongsi (Shenzhen Kaiwendi Trading Co., Ltd.), dba Eokeanon, of China

  Svnntaa 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. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. Furthermore, the bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.

  Unclassified

• Medical Device Recall · May 7, 2026

  AVID Medical, Inc.

  Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.

  Incorrect concentration of Betadine solution contained within certain AVID convenience kits.

  Class II

• Consumer Product Recall · May 7, 2026

  Allura Imports Inc., of New York, New York

  Youth Sweatshirts with Drawstrings

  The drawstrings in the recalled clothing can get caught on objects and cause death or serious injury to children from strangulation. The sweatshirts are in violation of the federal regulations for children's upper outerwear and present a substantial product hazard.

  Unclassified

• Consumer Product Recall · May 7, 2026

  EEMB USA, doing business as A2batt, Inc., of Redlands, California

  EEMB Lithium Battery Packs

  The lithium coin batteries are in pouches that are not child-resistant as required under Reese's Law. If a child swallows button cell or coin batteries, the ingested batteries can cause serious injuries, including internal chemical burns and death.

  Unclassified

• Consumer Product Recall · May 7, 2026

  Foshan Kangzhibao Furniture Co., Ltd. (doing business as EVLWZL) of China

  EVLWZL and Gunugu Mattresses

  The mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.

  Unclassified

• Consumer Product Recall · May 7, 2026

  Shenzhenshilingkexunkeji Co., Ltd. (Shenzhen Lingkexun Technology Co., Ltd.), dba Foubeaka and Geniuss, of China

  Multi-Purpose Helmets

  The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the positional stability and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

  Unclassified

• Medical Device Recall · May 7, 2026

  Draeger, Inc.

  Atlan A350XL. Model Number: 8621600. anesthesia workstation

  The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

  Class I

• Medical Device Recall · May 7, 2026

  TELEFLEX LLC

  Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton) Model/Catalog Number: 200100 200101 200102 200103 200104 200105

  Due to out-of-specification, or potential out-of-specification, levels of endotoxins

  Class II

• Food Recall · May 7, 2026

  Llorens Pharmaceuticals International Division, Inc.

  Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400 bottle, 47 SERVING PER BOTTLE, 24 bottles- 8 FL Oz (237mL) Amber PET modern round bo

  Foreign object: black particulate matter

  Class II

• Food Recall · May 6, 2026

  Albertsons Companies LLC

  UPC 23180100000 SHRIMP KABOB 16-20 CT W/KUNG PAO MRND This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.

  Contains statement does not declare Shrimp.

  Class III