Safety Recalls
RSS ↗15,264 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 5,651–5,700 of 15,264
- Class II
Drug Recall · July 9, 2025
Rizatriptan Benzoate Tablets, USP, 5 mg, 18 (3x6) Unit Dose Tablets, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories LLC, Parsippany, NJ 07054, NDC 67877-CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
- Class II
Medical Device Recall · July 9, 2025
Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number: 341-16-704 Product Description: Enovis knee devices are intended for treatment oKnee implants contain incorrect labeling (size and/or side incorrect)
- Class II
Drug Recall · July 9, 2025
Rizatriptan Benzoate Tablets, USP, 10 mg, 18 (3x6) Unit Dose Tablets, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories LLC, Parsippany, NJ 07054, NDC 67877CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
- Class I
Medical Device Recall · July 9, 2025
Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.Label is incorrect. The product label indicates that the device contains an air eliminating filter. However, the filter utilized on this extension set is not indicated for removal of air and does not feature an air vent, which is common to air eliminating filters.
- Class I
Food Recall · July 8, 2025
Sheehan Brothers Vending Cheeseburger, 4.7 oz (132g), individually wrapped in plastic, UPC: 100000952375Undeclared sesame
- Class I
Medical Device Recall · July 8, 2025
BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 SmartSite Y-sites LVP 60D DEHP FREE 3SS CV; REF: 2452-0007, BD Alaris Pump Infusion Set, 2 Back CheckInfusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
- Class II
Food Recall · July 8, 2025
Ritz Peanut Butter Cracker Sandwiches, Net Wt. 11.4 oz, 8 count (8x1.38 oz 6 pack of cracker sandwiches inside carton. 14X8-Case: 14 - 11.04 Oz Cartons in master carton. UPC 0 44000 88210 5Undeclared allergens (Peanut) due to mispackaging
- Class II
Food Recall · July 8, 2025
Ritz Cracker Sandwiches, Variety 20 count variety Pack, (20- Packs of 10 Cheese 1.35 oz Packs and 10 Peanut Butter 1.38 oz Packs) Net Wt. 27.3 oz (20-1.38 oz packet of cracker sandwiches inside cartonUndeclared allergens (Peanut) due to mispackaging
- Class II
Food Recall · July 8, 2025
Ritz Peanut Butter Cracker Sandwiches, Net Wt. 55.2 oz, 40 count (40x1.38 oz 6 pack of cracker sandwiches inside carton. 40 - 55.2oz Cartons in master carton. UPC 0 44000 07819 5Undeclared allergens (Peanut) due to mispackaging
- Class II
Medical Device Recall · July 8, 2025
Boston Scientific Neuromodulation Corporation
Vercise Deep Brain Stimulation Systems Surgical Implant Manual, Document Number: 92328632-09Wire break(s) have occurred in rechargeable deep brain stimulation implantable pulse generators, implanted in the submuscular pectoral location. Wire breaks prevent successful stimulation, thus requiring device removal/replacement and users may experience high monopolar impedances, undesired sensation, loss of therapy, return of symptoms and/or Bluetooth connectivity challenges.
- Class II
Medical Device Recall · July 8, 2025
MEDLINE INDUSTRIES, LP - Northfield
The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals utilizing them. The kit is provided sterile, single-use and includes a range of compoAffected kits contain recalled Stryker Color Cuff Sterile Disposable Tourniquet Cuffs. Stryker Instruments initiated this recall due to a potential manufacturing defect in which the flange may detach from the bladder at the welded connection point. This detachment compromises the cuff's ability to maintain adequate air pressure, potentially resulting in tourniquet failure and increased risk of patient hemorrhaging.
- Class I
Food Recall · July 8, 2025
Sheehan Brothers Vending Spicy Chicken Sandwich, 6.5 oz (184g), individually wrapped in plastic, UPC: 100000222539Undeclared sesame
- Class II
Medical Device Recall · July 8, 2025
Becton, Dickinson and Company, BD Bio Sciences
BD Trucount Controls, 30 Test - REF: 664343, RxOnly, IVDControl kits contain incorrect standard deviation (SD) values for the low and high control beads which compromises the accurate calculation of bead counts.
- Class II
Medical Device Recall · July 8, 2025
Becton, Dickinson and Company, BD Bio Sciences
BD Trucount Controls, 30 Test - REF: 340335Control kits contain incorrect standard deviation (SD) values for the low and high control beads which compromises the accurate calculation of bead counts.
- Class I
Food Recall · July 8, 2025
Sheehan Brothers Vending Italian Mini Sub, 6.1 oz (174g), in a brown paper boat and individually wrapped in plastic, UPC: 100000952412Undeclared sesame
- Class I
Medical Device Recall · July 8, 2025
BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versionsInfusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
- Class I
Food Recall · July 8, 2025
Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw, 8 oz (226g), in a plastic tray/2 oz cup and individually wrapped in plastic, UPC: 100000222744Undeclared sesame
- Class II
Medical Device Recall · July 8, 2025
Boston Scientific Neuromodulation Corporation
Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep Stimulation System used with the Surgical Implant ManualResistance and difficulties could occur while closing the retaining clip locking mechanism, which is part of a burr hole cover kit, which is part of a Deep Brain Stimulation (DBS) system, which may lead to procedural delay, or lead-migration-which may require additional surgery.
- Unclassified
Vehicle Recall · July 8, 2025
2025 NISSAN FRONTIERDaytime running lights that dim unexpectedly may cause confusion to other vehicles or pedestrians, increasing the risk of a crash.
- Class I
Food Recall · July 8, 2025
Sheehan Brothers Vending Chili Cheese Coney, 4.3 oz (120g), in a red and white paper boat and individually wrapped in plastic, UPC: 100000222027Undeclared sesame
- Class II
Food Recall · July 8, 2025
Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside cartons. And 6x20(6 - 27.6 oz Cartons) in master carton. UPC 1 00 44000 07584 2Undeclared allergens (Peanut) due to mispackaging
- Class I
Food Recall · July 8, 2025
Sheehan Brothers Vending Pepperoni Pizza Mini Sub, 4.8 oz (136g), in a brown paper boat and individually wrapped in plastic, UPC: 100000222584Undeclared sesame
- Class II
Drug Recall · July 7, 2025
MEDLINE INDUSTRIES, LP - Northfield
Good Neighbor Pharmacy, Alcohol Prep Pads, Distributed By AmeriSource Bergen, 1 West First Avenue, Conshohocken, PA 19428, Made in China: 100 eaches per box, 30 boxes per case, (3,000 eaches per case)Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
- Class I
Medical Device Recall · July 7, 2025
Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent, stent and stent delivery system. Material numbers: H7493915010240 CAROTID WALLSTENT MONORAIL 10.0-24; H7493915010310Certain batches are being removed due to an increase in complaints received in which physicians encountered greater than anticipated resistance while attempting to withdraw the stent delivery system (SDS) from the guidewire or embolic protection device (EPD) after successful stent deployment. The most serious potential adverse health consequence is stroke. Other risks include delay to procedure, vessel injury, vessel spasm, or stent disruption/damage necessitating additional intervention.
- Class II
Drug Recall · July 7, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only, Large, www.medline.com, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093 USA,Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
- Unclassified
Vehicle Recall · July 7, 2025
2023 FORD BRONCO, 2023 FORD EXPLORER, 2023 FORD F-250 SD, 2023 FORD F-350 SD, 2023 FORD F-550 SD, 2023 FORD F-450 SD, 2023 LINCOLN AVIATORAn engine stall increases the risk of a crash.
- Class II
Drug Recall · July 7, 2025
MEDLINE INDUSTRIES, LP - Northfield
CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per Case, Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093, USASubpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
- Unclassified
Vehicle Recall · July 7, 2025
Jaguar Land Rover North America, LLC
2023 LAND ROVER RANGE ROVER EVOQUE, 2024 LAND ROVER RANGE ROVER EVOQUEA torn air bag may not adequately protect an occupant in a crash, increasing the risk of injury. Additionally, a torn air bag may allow hot gases to escape, which can cause a burn injury.
- Unclassified
Vehicle Recall · July 7, 2025
2025 POLESTAR POLESTAR 3Damage to harnesses can cause various electrical malfunctions, such as a loss of power steering assist, increasing the risk of a crash or injury.
- Unclassified
Vehicle Recall · July 7, 2025
2024 KAWASAKI NINJA ZX-6R, 2025 KAWASAKI NINJA ZX-6RAn engine stall increases the risk of a crash.
- Class II
Drug Recall · July 7, 2025
MEDLINE INDUSTRIES, LP - Northfield
ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs, Distributed by, Walmart, Inc., Bentonville, AR 72716 Walmart: 200 eaches per box, 24 boxes per case (4,800 eaches per case), NDC 49035-814-60.Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
- Class II
Drug Recall · July 7, 2025
MEDLINE INDUSTRIES, LP - Northfield
RITE AID PHARMACY, first aid alcohol prep pads, DISTRIBUTED BY: RITE AID. 200 NEWBERRY COMMONS, ETTERS, PA 17319, NDC 11822-5156-2.Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
- Class II
Drug Recall · July 7, 2025
MEDLINE INDUSTRIES, LP - Northfield
H-E-B, inControl, Sterile* Alcohol Pads, CONT. 100 PADS, Packaged in China with components from Taiwan, Elaborado Con Orgullo Y Cuidado PARA H-E-B, San Antonio, TX 78204, NDC 37808-809-09.Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
- Class II
Food Recall · July 7, 2025
J. Higgs Potato Chip Mix, 18 1oz singles, net weight 180z., UPC 0-51933-37327-3undeclared milk
- Class II
Medical Device Recall · July 7, 2025
Siemens Healthcare Diagnostics Inc
epoc BGEM BUN Test Card [25pk]. Material Number: 10736515.Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium bias may exist in some epoc test card lots. All other analytes are performing as intended. The observed average bias for sodium was -4.4 mmol/L. The maximum bias observed was -14 mmol/L, which occurred at a higher sodium concentration around 150 mmol/L. No positive bias has been observed. Quality Control (QC) fluid may or may not detect the issue depending on the bias magnitude and the frequency of QC testing.
- Unclassified
Vehicle Recall · July 5, 2025
Volkswagen Group of America, Inc.
2023 AUDI Q5, 2024 AUDI Q5The screws can loosen, allowing oil to leak and increasing the risk of a fire.
- Class II
Drug Recall · July 5, 2025
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New JerseDefective Container: spike of the cap becomes lodged in the nozzle of the product bottle.
- Unclassified
Vehicle Recall · July 5, 2025
Daimler Trucks North America, LLC
2025 FREIGHTLINER CASCADIA, 2025 FREIGHTLINER BUSINESS CLASS M2Reduced brake performance can extend the distance required to stop, increasing the risk of a crash.
- Unclassified
Vehicle Recall · July 5, 2025
2025 POLESTAR POLESTAR 3A rearview camera image that does not display reduces the driver's view of what is behind the vehicle, increasing the risk of a crash.
- Unclassified
Vehicle Recall · July 4, 2025
2023 NOVA BUS LFSA loss of drive power can increase the risk of a crash.
- Class III
Medical Device Recall · July 3, 2025
L8-4 Transducer ProbeTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- Class III
Medical Device Recall · July 3, 2025
C9-4 Transducer ProbeTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- Class III
Medical Device Recall · July 3, 2025
C5-2 Lumify Transducer ProbeTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- Class III
Medical Device Recall · July 3, 2025
S5-2 Transducer ProbeTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- Class III
Medical Device Recall · July 3, 2025
mC7-2 Transducer ProbeTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- Class III
Medical Device Recall · July 3, 2025
C9-3v Transducer ProbeTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- Class III
Medical Device Recall · July 3, 2025
L15-7io Transducer ProbeTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- Class III
Medical Device Recall · July 3, 2025
OMNI III TEE Transducer ProbeTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.
- Class II
Medical Device Recall · July 3, 2025
Orascoptic Superior Visualization Custom loupes with Dragonfly framesDue to complaints, loupe nose pads containing nickel may cause an allergic reaction.
- Class III
Medical Device Recall · July 3, 2025
V9-2 Transducer ProbeTo provide clarification and labelling to define the useful life of ultrasound transducers in the field.