Safety Recalls

15,182 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 1,301–1,350 of 15,182

• Medical Device Recall · April 2, 2026

  DFI Co., Ltd.

  One Step P in vitro diagnostic test REF: 8194

  The devices were distributed without required FDA premarket clearance or approval.

  Class II

• Food Recall · April 2, 2026

  Raw Farm LLC

  RAW FARM SHREDDED RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204000194

  Multi-state outbreak of E. coli O157:H7.

  Class I

• Food Recall · April 2, 2026

  F&S Fresh Foods, Inc.

  ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich, perishable, Keep Refrigerated, plastic clamshell, net wt. 10 oz, UPC 8 26766 25036 3. Distributed By F&S Fresh Foods Vineland, NJ 08360. Label

  Undeclared sesame. Sandwich contains visible sesame but label does not declare sesame.

  Class II

• Food Recall · April 2, 2026

  HEMU TRADING INC

  Black label with blue lettering. FOOD Korean Food, ENOKI MUSHROOM, 150g clear plastic package; Product of Korea, Keep Refrigerated. Distributed by Hemu Trading Inc. UPC: 8801234567893

  product tested positive for Listeria Monocytogenes.

  Class I

• Consumer Product Recall · April 2, 2026

  E Mishan & Sons, Inc., of New York, New York

  Granitestone Diamond Pro Blue Sauté Pans

  The metal cap on the screw that connects the sauté pan to the handle can become detached and forcefully eject when heated, posing impact and burn hazards to consumers.

  Unclassified

• Consumer Product Recall · April 2, 2026

  Fuzhou Shiahaha Cultural Industry Development Co., Ltd., of China

  ELENKER Bed Rails

  The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, 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 2, 2026

  Shenzhen Weichaoda Technology Co., Ltd., dba CSZWEICD, of China

  Gavoyeat Halloween Light-Up Rings Party Favors

  The recalled light-up rings violate the mandatory safety standard for toys because the battery compartment within the LED light ring contains button cell batteries that can be easily accessed by children. 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 2, 2026

  Hansoll Textile Ltd., of South Korea

  Member's Mark Children's Valentine SS Notch Collar Pajama Sets

  The recalled pajama sets violate the mandatory standards for flammability of children's sleepwear, posing a risk of burn injuries to children.

  Unclassified

• Consumer Product Recall · April 2, 2026

  Jichehui Electronics Co. Ltd., dba TecFlox, of China

  TecFlox Hair and Beard Growth Serum Bottles

  The hair and beard growth serum contains minoxidil, 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 · April 2, 2026

  DrHealBeauty, of Japan

  Tuymec Minoxidil Hair Growth Kits, 5% Minoxidil with Biotin Spray

  The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.

  Unclassified

• Medical Device Recall · April 1, 2026

  Aniara Diagnostica LLC

  ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A

  Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.

  Class II

• Medical Device Recall · April 1, 2026

  BioFire Diagnostics, LLC

  Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485

  Respiratory/sore throat panel test may result in false negative results and control failures.

  Class II

• Drug Recall · April 1, 2026

  Wells Pharma of Houston LLC

  Phenylephrine Hydrochloride Injectable Solution, 40mg, 250*mL Bag, wells pharma of Houston, NDC 73702-122-03

  cGMP deviations.

  Class II

• Medical Device Recall · April 1, 2026

  Abbott Point Of Care Inc.

  i-STAT EG7+ cartridge; List Number: 03P76-25;

  Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.S. marketplace may report higher than expected PCO2 and lower than expected pH results due to a manufacturing issue. A falsely high pCO2 together with a falsely low pH makes the blood gas appear as if the patient is in severe respiratory acidosis. If the clinician believes the values are real, it may trigger unnecessary or even harmful interventions such as unnecessary ventilator changes, unnecessary medications, potential harm from overcorrection, or delays in identifying true problems.

  Class II

• Drug Recall · April 1, 2026

  Wells Pharma of Houston LLC

  Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.

  cGMP deviations.

  Class II

• Drug Recall · April 1, 2026

  Wells Pharma of Houston LLC

  fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, NDC 73702-203-65.

  cGMP deviations.

  Class II

• Drug Recall · April 1, 2026

  Wells Pharma of Houston LLC

  fentaNYL Citrate injectable Solution in 0.9% Sodium Chloride, Narcotic, (2500 mcg/ 250 mL) (10 mcg per mL), 250 mL bag, wells pharma of Houston, NDC 73702-202-03.

  cGMP deviations.

  Class II

• Medical Device Recall · April 1, 2026

  Abbott Point Of Care Inc.

  i-STAT EG6+ cartridge; List Number: 03P77-25;

  Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.S. marketplace may report higher than expected PCO2 and lower than expected pH results due to a manufacturing issue. A falsely high pCO2 together with a falsely low pH makes the blood gas appear as if the patient is in severe respiratory acidosis. If the clinician believes the values are real, it may trigger unnecessary or even harmful interventions such as unnecessary ventilator changes, unnecessary medications, potential harm from overcorrection, or delays in identifying true problems.

  Class II

• Drug Recall · April 1, 2026

  International Medication Systems Ltd.

  EPINEPHRINE Injection, USP, 1 mg/10mL (0.1 mg/mL), Rx only, INTERNATIONAL MEDICATION SYSTEMS, LIMITED, So. EL Monte, CA 91733, An Amphastar Pharmaceutical Company, NDC 76329-3318-1

  Lack of Assurance of Sterility

  Class II

• Drug Recall · April 1, 2026

  Wells Pharma of Houston LLC

  fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houston, NDC 73702-202-02.

  cGMP deviations.

  Class II

• Drug Recall · April 1, 2026

  Wells Pharma of Houston LLC

  fentaNYL Citrate Injectable Solution, Narcotic, CII, 1250 mcg/25mL (50 mcg per mL), 25 mL, wells pharma of Houston, NDC 73702-204-25.

  cGMP deviations.

  Class II

• Medical Device Recall · April 1, 2026

  Abbott Point Of Care Inc.

  i-STAT G3+ cartridge; List Number: 03P78-26;

  Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.S. marketplace may report higher than expected PCO2 and lower than expected pH results due to a manufacturing issue. A falsely high pCO2 together with a falsely low pH makes the blood gas appear as if the patient is in severe respiratory acidosis. If the clinician believes the values are real, it may trigger unnecessary or even harmful interventions such as unnecessary ventilator changes, unnecessary medications, potential harm from overcorrection, or delays in identifying true problems.

  Class II

• Drug Recall · April 1, 2026

  Wells Pharma of Houston LLC

  fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 50 mcg/5mL)(10 mcg per mL), wells pharma, NDC 73702-202-15.

  cGMP deviations.

  Class II

• Drug Recall · April 1, 2026

  Island Kinetics, Inc. d.b.a. CoValence Laboratories

  Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873 9.

  Failed Stability Specifications

  Class II

• Food Recall · April 1, 2026

  PURE PALM C/O DVD

  Label is predominantly green with white lettering in a clear plastic clamshell container. Pure Palm dates- Medjool Dates Net Wt. 16OZ UPC: 852160007005

  mislabeled Coconut Date Bites. (product is coconut covered, label is for regular date bites)

  Class II

• Medical Device Recall · March 31, 2026

  Erbe Medical, LLC

  ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222

  Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water flow from distal tip under unsupported third-party connector use conditions, which may lead to water aspiration, which may progress to aspiration pneumonia, acute respiratory distress syndrome, or respiratory failure.

  Class II

• Medical Device Recall · March 31, 2026

  Erbe Medical, LLC

  ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2 Tubing/Cap Set for Olympus Scopes & UCR, REF: 20325-240; Hybrid CO2 Tubing/Cap Set for Oly

  Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water flow from distal tip under unsupported third-party connector use conditions, which may lead to water aspiration, which may progress to aspiration pneumonia, acute respiratory distress syndrome, or respiratory failure.

  Class II

• Medical Device Recall · March 31, 2026

  PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

  Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230), Azurion 5 (722281), Azurion 5 M12 (722227, 722231), Azurion 5 M20 (722228, 7222

  Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to the forces applied when the monitor is moved or rotated.

  Class II

• Drug Recall · March 31, 2026

  Avantor Performance Materials LLC

  Magnesium Chloride, 6-Hydrate, Crystal, 500G per bottle, Bulk active pharmaceutical ingredient (API), Avantor Performance Materials, LLC, 100 Matsonford Road, Suite 200, Radnor, PA 19087, NDC 10106-24

  Subpotent drug

  Class III

• Medical Device Recall · March 31, 2026

  Erbe Medical, LLC

  ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes, 20325-201; ERBEFLO CleverCap Hybrid Tubing/Cap Set for Fujifilm Scopes, REF: 20325-203;

  Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water flow from distal tip under unsupported third-party connector use conditions, which may lead to water aspiration, which may progress to aspiration pneumonia, acute respiratory distress syndrome, or respiratory failure.

  Class II

• Food Recall · March 30, 2026

  HEYTEA USA INC

  Coconut Drink 1; NET VOLUME: 1L; Ingredients: Coconut water, freshly squeezed coconut gravy, white granulated sugar, emulsion stabilizer [sodium caseinate, mono- and diglycerides fatty acid esters, su

  Product contains undeclared milk.

  Class II

• Medical Device Recall · March 30, 2026

  Boston Scientific Corporation

  LUX-Dx II Plus, Arrythmia detector and alarm, Model M312, with SERVER SW LATITUDE DRAGON EU (Europe), Model 6446, Version 7.5, or SERVER SW LATITUDE DRAGON AU (Australia/New Zealand), Model 6448, Vers

  For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring for Bradyarrhythmia and Pause (M312 only). In addition, for these devices that are not being monitored, the LATITUDE Clarity programming screens have discrepant information, indicating that the monitoring is enabled for these features in one location and not enabled in another location.

  Class II

• Medical Device Recall · March 30, 2026

  Zimmer, Inc.

  Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number: 00-5049-011-00 Software Version: N/A Product Description: Mixing Bowl and Spatula Comp

  Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or peeling seals. Compromised sterile barrier may lead to clinically insignificant extension of surgery or infection leading to surgical intervention.

  Class II

• Medical Device Recall · March 30, 2026

  Boston Scientific Corporation

  LUX-DX II, Arrythmia detector and alarm, Model M302, with SERVER SW LATITUDE DRAGON US, Model 6460, Version 7.5

  For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring for Bradyarrhythmia and Pause (M312 only). In addition, for these devices that are not being monitored, the LATITUDE Clarity programming screens have discrepant information, indicating that the monitoring is enabled for these features in one location and not enabled in another location.

  Class II

• Medical Device Recall · March 27, 2026

  Edwards Lifesciences, LLC

  Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO

  Labeling update to provide warning if functionality of the valve replacement delivery system is compromised.

  Class II

• Drug Recall · March 27, 2026

  Appco Pharma LLC

  Prazosin Hydrochloride Capsules, USP, 2mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ, Manufactured by: Appco Pharma LLC, Piscataway, NJ, NDC 70377-067-11.

  cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.

  Class II

• Medical Device Recall · March 27, 2026

  Straumann USA LLC

  Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments

  Includes an incorrect screw seat interface.

  Class II

• Drug Recall · March 27, 2026

  Appco Pharma LLC

  Prazosin Hydrochloride Capsules, USP, 5mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ, Manufactured by: Appco Pharma LLC, Piscataway, NJ, NDC 70377-068-11.

  cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.

  Class II

• Medical Device Recall · March 27, 2026

  Straumann USA LLC

  Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments

  Includes an incorrect screw seat interface.

  Class II

• Drug Recall · March 27, 2026

  Appco Pharma LLC

  Prazosin Hydrochloride Capsules, USP, 1mg, 100-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ, Manufactured by: Appco Pharma LLC, Piscataway, NJ, NDC 70377-066-11.

  cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.

  Class II

• Medical Device Recall · March 27, 2026

  North American Rescue LLC.

  AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits designed for the appropriate level provider to evaluate and treat patients at th

  Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the meter displays an E-5 error code for a very high blood glucose event (> 600 mg/dL) or when there is a test strip error, which can lead to operator confusion when evaluating patients and a delay in appropriate treatment. This is a downstream recall of Trividia Health Class I, Recall Event ID 98317.

  Class I

• Medical Device Recall · March 27, 2026

  Micro-X Ltd.

  Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71

  X-Ray generator may malfunction resulting in the X-Ray being inoperable.

  Class II

• Food Recall · March 27, 2026

  Blueroot Health, Inc.

  Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count bottles

  Contains undeclared egg, soy, and hazelnut

  Class II

• Medical Device Recall · March 26, 2026

  Spacelabs Healthcare, Inc.

  Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model/Catalog Number: 91496 Software Version: N/A Product Description: The Command Module (91496) is the core of t

  Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester).

  Class II

• Medical Device Recall · March 26, 2026

  GE Medical Systems, LLC

  Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300

  GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.

  Class II

• Consumer Product Recall · March 26, 2026

  Nexgrill Industries, Inc. of Chino, California

  Metal Wire Bristle Grill Brushes

  Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.

  Unclassified

• Consumer Product Recall · March 26, 2026

  Shenzhen City Donglin E-Commerce Co., Ltd d/b/a 4our Kiddies, of China

  4our Kiddies Plastic Tip Restraint Kits

  The recalled plastic tip restraint kits (also referred to as furniture straps) can break or degrade, posing tip-over and entrapment hazards that can result in serious injuries or death to children or elderly consumers interacting with furniture that is secured to the wall with the defective plastic tip restraints. This is a hidden defect because consumers who purchase and install this product may be under a false sense of security that their furniture is safe from a tip-over incident.

  Unclassified

• Consumer Product Recall · March 26, 2026

  Plunge Buddy LLC, doing business as DIY Cold Plunge, of North Mankato, Minnesota

  DIY Sauna Heater Kits

  Electrical conductors within the sauna heater kits can overheat, posing a fire hazard and risk of serious injury or death.

  Unclassified

• Consumer Product Recall · March 26, 2026

  Shenzhen Jiaying E-commerce Co., Ltd., dba GLMZZ, of China

  GLMZZ Fidget Magnet Ball Toys

  The magnet ball toys violate the mandatory standard for toys because they are high-powered magnets, posing an ingestion hazard to children. When high-powered magnets are swallowed, they 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 · March 26, 2026

  Vive Health LLC, of Naples, Florida

  Vive Health Bed Rails

  When the recalled bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress. This poses a serious entrapment hazard and risk of death by asphyxiation.

  Unclassified