Safety Recalls

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

Showing 1,751–1,800 of 17,553

• Consumer Product Recall · May 14, 2026

  BRP US Inc., of Sturtevant, Wisconsin

  Can-Am Outlander Pro and Max Pro All-Terrain Vehicles

  The ATV's speed limiter control can malfunction, causing unexpected speed and acceleration, posing a serious risk of injury or death from crash hazard.

  Unclassified

• Vehicle Recall · May 14, 2026

  Honda (American Honda Motor Co.)

  2024 ACURA ZDX

  A rearview image that does not display correctly reduces the driver's view behind the vehicle, increasing the risk of a crash or injury.

  Unclassified

• Consumer Product Recall · May 14, 2026

  Minka Lighting Group, LLC, of Corona, California

  Minka Bardon Series Pendant Light Fixtures

  The recalled light fixture's frame can detach from the pendant downrod during installation, posing a risk of serious injury or death from an impact hazard.

  Unclassified

• Consumer Product Recall · May 14, 2026

  Missry Associates Inc., doing business as Misco Enterprises, of Edison, New Jersey

  Misco Sports Badminton Toy Sets Red/Blue MT2383

  The Misco Sports Badminton Toy Sets violate the mandatory safety standard for children's toys because the shuttlecocks contain 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 deaths.

  Unclassified

• Consumer Product Recall · May 14, 2026

  Guidecraft, of Mocksville, North Carolina

  Guidecraft Kitchen Helper Towers

  The platform inside the recalled tower can loosen over time, causing it to become unstable or detach, and ultimately posing a fall hazard to young children.

  Unclassified

• Consumer Product Recall · May 14, 2026

  Guangzhou Lichengbei Battery Technology Co., Ltd., dba LiCB, of China

  LiCB CR2032 3V Lithium Coin Batteries

  The recalled coin batteries are not in child-resistant packaging and do not bear the warning labels 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

• Drug Recall · May 14, 2026

  AVEVA Drug Delivery Systems, Inc.

  Nicotine Transdermal System Patch, 14 mg, 14 patches per box, Aveva, Distributed by: RUGBY LABORATORIES, Indianapolis, IN 46268, www.majorpharmaceuticals.com, NDC 0536-5895-88.

  Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of individual units.

  Class III

• Consumer Product Recall · May 14, 2026

  Generac Power Systems Inc., of Waukesha, Wisconsin

  Electric Start Pressure Washers

  The electronic start/stop button on the pressure washer can malfunction and self-start, posing a risk of serious injury or death due to carbon monoxide poisoning, if the unit is in a confined space.

  Unclassified

• Consumer Product Recall · May 14, 2026

  Zhongwan Guangzhou Technology Co., Ltd (Zhongwan Guangzhou Kejiyouxiangongsi), dba ZW Creations, of China

  Tiyol Pull String Teething Toys

  The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The silicone strings can reach the back of the throat and become lodged, posing a risk of respiratory distress and becoming a deadly choking hazard.

  Unclassified

• Consumer Product Recall · May 14, 2026

  Costco Wholesale Corporation, of Issaquah, Washington

  Agio Menlo Woven Patio Swings

  The swing seat can detach from the frame while in use, posing a risk of serious injury or death from a fall hazard.

  Unclassified

• Consumer Product Recall · May 14, 2026

  ZWILLING J.A. Henckels Aktiengesellschaft, Solingen, Germany

  Electric Kettles (ENFINIGY 1.5 l and ENFINIGY Pro 1.5 l)

  The kettle's handle can loosen and separate from the kettle, causing hot contents to spill, posing a risk of serious injury due to a burn hazard.

  Unclassified

• Medical Device Recall · May 14, 2026

  ConMed Corporation

  ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Lapar

  Potential for overpressure alerts.

  Class II

• Medical Device Recall · May 14, 2026

  ConMed Corporation

  ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS5-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxid

  Potential for overpressure alerts.

  Class II

• Drug Recall · May 14, 2026

  Asclemed USA Inc.

  Duloxetine DR Capsules, 30 mg, 30 count bottles, Rx, Relabeled by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC 76420-634-30, Marketed by: Ajanta Pharma USA Inc.

  CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.

  Class II

• Food Recall · May 14, 2026

  United Salt Corp

  Salt

  Plain salt was labeled as iodized and iodized salt was labeled as plain.

  Class III

• Food Recall · May 13, 2026

  Nutrisystem Inc

  Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow Wrapped, 48 units per case, Keep frozen

  Undeclared Allergen (Soy)

  Class II

• Food Recall · May 13, 2026

  Terra Medi LLC

  Hellas Meze Golden Smoked Whole Herring

  Un-eviscerated fish may be contaminated with clostridium botulinum

  Class I

• Medical Device Recall · May 13, 2026

  Alphatec Spine, Inc.

  SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System

  Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system faults, loss of communication between the Patient Interface and Tablet, and prompts requiring system reboot; may result in increased operative time and surgical plan change.

  Class II

• Medical Device Recall · May 13, 2026

  Thoratec LLC

  Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery, ABT Model/Catalog Number: 106128 Software Version: N/A Product Description: The HeartMate 11 Volt Lithium Ion Standalone Backup Ba

  Due to 11 volt Backup Battery failures.

  Class II

• Medical Device Recall · May 13, 2026

  Medtronic Neuromodulation

  Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor

  A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

  Class II

• Medical Device Recall · May 13, 2026

  Medical Action Industries, Inc. 306

  Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds

  Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within blood vessels.

  Class I

• Vehicle Recall · May 13, 2026

  Lucid USA, Inc.

  2024 LUCID AIR, 2025 LUCID AIR

  A loss of drive power increases the risk of a crash.

  Unclassified

• Medical Device Recall · May 13, 2026

  Covidien, LLC

  EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1 10884521808096 05391530810166 DL ENDOFLIP 1 10884521786684 Endosc

  The system's 24-hour usage limit results in catheters incorrectly flagged as expired, making them unavailable for clinical procedures.

  Class II

• Medical Device Recall · May 13, 2026

  Medtronic Neuromodulation

  Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor

  A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

  Class II

• Medical Device Recall · May 13, 2026

  Thoratec LLC

  Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog Number: 106531US Software Version: N/A Product Description: The HeartMate 3" System Controller acts as the central

  Due to 11 volt Backup Battery failures.

  Class II

• Medical Device Recall · May 13, 2026

  Thoratec LLC

  Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assi

  Due to 11 volt Backup Battery failures.

  Class II

• Food Recall · May 13, 2026

  CERELES EN GENERAL SAS

  Pearl Milling Company Original Pancake & Waffle Mix Complete (Mezcla Para Panqueques y Waffles) Net Wt 5.99 oz (170 g). Packed in 50 - 5.99 oz BOPP Pouch units per master case. Keep in a cool, dry pla

  Undeclared allergens: Milk and Soy

  Class I

• Medical Device Recall · May 12, 2026

  ICU Medical, Inc.

  IV Sets with drip chambers

  Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.

  Class II

• Food Recall · May 12, 2026

  Straus Family Creamery

  STRAUS FAMILY CREAMERY Strawberry ORGANIC SUPER PREMIUM ICE CREAM ONE QUART (946mL) ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC for QUART: 7848301009

  Potential contamination with foreign objects (metal pieces).

  Class II

• Drug Recall · May 12, 2026

  IntegraDose Compounding Services LLC

  fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3650 Victorie St N, Suite 900, Shoreview, MN, NDC 71139-6030-1.

  Subpotent Drug

  Class II

• Drug Recall · May 12, 2026

  Spectra Medical Devices, Llc

  Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC, Wilmington, Made in S. Korea, NDC 65282-1605-1.

  Lack of Assurance of Sterility

  Class II

• Medical Device Recall · May 12, 2026

  Medtronic Perfusion Systems

  Octopus 4 Tissue Stabilizer, Model 29400

  During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

  Class II

• Vehicle Recall · May 12, 2026

  Nova Bus (US) Inc.

  2023 NOVA BUS LFS

  A missing DOT code mark may result in the door being replaced with the incorrect type of plastic, reducing visibility and increasing the risk of a crash.

  Unclassified

• Medical Device Recall · May 12, 2026

  Medtronic Perfusion Systems

  Octopus Evolution AS Tissue Stabilizer, Model TS2500

  During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

  Class II

• Medical Device Recall · May 12, 2026

  ICU Medical, Inc.

  Plum administration sets

  Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.

  Class II

• Medical Device Recall · May 12, 2026

  Abbott Medical

  Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software

  Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.

  Class II

• Medical Device Recall · May 12, 2026

  ICU Medical, Inc.

  IV Sets with drip chambers

  Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.

  Class II

• Medical Device Recall · May 12, 2026

  ICU Medical, Inc.

  IV Sets with drip chambers

  Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.

  Class II

• Medical Device Recall · May 12, 2026

  ICU Medical, Inc.

  IV Non-Dedicated Gravity Administration Sets with drip chambers

  Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall that does not enter the fluid path, which if seen by a healthcare provider may lead to replacement of product before use, which could result in a delay in therapy.

  Class II

• Medical Device Recall · May 12, 2026

  Medtronic Perfusion Systems

  Octopus Evolution Tissue Stabilizer, Model TS2000

  During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

  Class II

• Medical Device Recall · May 12, 2026

  ICU Medical, Inc.

  Oncology sets with drip chambers

  Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall that does not enter the fluid path, which if seen by a healthcare provider may lead to replacement of product before use, which could result in a delay in therapy.

  Class II

• Drug Recall · May 12, 2026

  ANI Pharmaceuticals, Inc.

  Estradiol Gel, 0.1%, 0.25 mg, 0.25 g per packet, 30 packets per carton, Rx only, Distributed by: ANI Pharmaceuticals, Inc., Baudette, MN 56623. NDC 70954-531-20

  Defective Container; packets were found to be either empty or partially full.

  Class II

• Drug Recall · May 12, 2026

  SUN PHARMACEUTICAL INDUSTRIES INC

  DOXOrubin Hydrochloride Liposome injection, 50 mg/25 mL (2mg/mL), 25 mL single-dose vials, Sterile, Rx only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, Manufactured by: Sun Pharmaceutical

  Presence of Particulate matter: Particulate matter identified as glass.

  Class I

• Food Recall · May 12, 2026

  Straus Family Creamery

  STRAUS FAMILY CREAMERY Mint Chip ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830100504

  Potential contamination with foreign objects (metal pieces).

  Class II

• Food Recall · May 12, 2026

  Straus Family Creamery

  STRAUS FAMILY CREAMERY Cookie Dough ORGANIC SUPER PREMIUM ICE CREAM ONE PINT (473mL) Produced and Distributed by Straus Family Creamery, Petaluma, CA 94952 UPC: 784830101044

  Potential contamination with foreign objects (metal pieces).

  Class II

• Medical Device Recall · May 12, 2026

  ICU Medical, Inc.

  IV Sets with drip chambers

  Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.

  Class II

• Medical Device Recall · May 12, 2026

  Fresenius Medical Care Holdings, Inc.

  Bicarby" Dialysate; Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G;

  Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-lock leaks during manipulation of the frangible and tubing when preparing the product for use for treatment. This issue presents the potential of a slip and fall hazard associated with fluid on the floor.

  Class II

• Medical Device Recall · May 12, 2026

  Boston Scientific Corporation

  Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastroint

  Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button sticking.

  Class II

• Food Recall · May 12, 2026

  Dkiru LLC

  Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net weight: 11.36 ounces. Serving size: 2 gummies. UPC: 860008784551 Firm name and address listed on label: Dkiru Ltd,

  Undeclared melatonin.

  Class II

• Medical Device Recall · May 12, 2026

  ICU Medical, Inc.

  Oncology sets with drip chambers

  Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall that does not enter the fluid path, which if seen by a healthcare provider may lead to replacement of product before use, which could result in a delay in therapy.

  Class II