Safety Recalls

15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 3,301–3,350 of 15,186

• Medical Device Recall · November 11, 2025

  Olympus Corporation of the Americas

  Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for urologic applications.

  Complaints of the ceramic tip of the resection sheath breaking have been received.

  Class II

• Food Recall · November 11, 2025

  The New York Milk Bank, Inc.

  Pasteurized Donor Human Milk in 4 ounce/120 ml clear plastic bottles. The bottles have a foil seal and are capped with a green lid. Bottle size: 120ml

  Foreign object

  Class II

• Drug Recall · November 11, 2025

  Dr. Reddy's Laboratories, Inc.

  Varenicline Tablets, 1mg, 56 Tablets, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 43598-908-56

  Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.

  Class III

• Food Recall · November 11, 2025

  Lexunder Inc

  Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 2 lb., 4 lb., 8 lb., 16 lb., and 44 lb. bags; Ingredients: ORGANIC MORINGA LEAF POWDER

  Contaminated with Salmonella

  Class I

• Food Recall · November 11, 2025

  Lexunder Inc

  Food to Live brand ORGANIC SUPERGREENS POWDER MIX, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 1.5 lb., 3 lb., 6 lb., 12 lb.; Ingredients: ORGANIC KALE; ORGANIC MORINGA LEAF; ORG

  Contaminated with Salmonella

  Class I

• Medical Device Recall · November 11, 2025

  Olympus Corporation of the Americas

  Olympus Resection Sheath, 24 Fr., with Deflecting Obturator; Model No. A22041T. Resection sheath for urologic applications.

  Complaints of the ceramic tip of the resection sheath breaking have been received.

  Class II

• Medical Device Recall · November 11, 2025

  Olympus Corporation of the Americas

  Olympus Inner Sheath; Model No. A2660. for endoscopic diagnosis and treatment in urological applications.

  Complaints of the ceramic tip of the resection sheath breaking have been received.

  Class II

• Medical Device Recall · November 11, 2025

  Olympus Corporation of the Americas

  Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for urologic applications.

  Complaints of the ceramic tip of the resection sheath breaking have been received.

  Class II

• Medical Device Recall · November 11, 2025

  AVID Medical, Inc.

  Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.

  Devices are not suitable for organ transplant.

  Class I

• Medical Device Recall · November 11, 2025

  Olympus Corporation of the Americas

  Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications.

  Complaints of the ceramic tip of the resection sheath breaking have been received.

  Class II

• Medical Device Recall · November 11, 2025

  AVID Medical, Inc.

  Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.

  Devices are not suitable for organ transplant.

  Class I

• Medical Device Recall · November 11, 2025

  Olympus Corporation of the Americas

  Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications.

  Complaints of the ceramic tip of the resection sheath breaking have been received.

  Class II

• Medical Device Recall · November 10, 2025

  Beckman Coulter, Inc.

  COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conjunction with a cyanide-free lytic agent for counting and sizing blood cells on all

  Due to specific lots of diluents contributing to elevated platelet Daily Checks background counts cycle with use with analyzers.

  Class II

• Food Recall · November 10, 2025

  Kosher First LLC

  Shloimy's Heimishe Matjes Herring packaged in 7oz plastic container

  Undeclared FD&C Red #40

  Class III

• Medical Device Recall · November 10, 2025

  Waldemar Link GmbH & Co. KG (Mfg Site)

  Endo Model Knee Fusion Nail SK, Knee Fusion Nail, Coupling Component, right, modular, L= 68 mm, Taper 10/12. Knee component of limb salvage replacement devices.

  The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.

  Class II

• Medical Device Recall · November 10, 2025

  Draeger, Inc.

  ErgoStar CM 55, Model/Catalog Number: MP01855, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a m

  Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.

  Class I

• Medical Device Recall · November 10, 2025

  Draeger, Inc.

  ErgoStar CM 45, Model/Catalog Number: MP01845, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a me

  Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.

  Class I

• Medical Device Recall · November 10, 2025

  Draeger, Inc.

  ErgoStar CM 60, Model/Catalog Number: MP01860, Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a m

  Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.

  Class I

• Medical Device Recall · November 10, 2025

  Draeger, Inc.

  ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction of respiratory gases between the breathing system and the patient interface. (e.g. endotracheal tube mask) of a mecha

  Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.

  Class I

• Vehicle Recall · November 9, 2025

  General Motors, LLC

  2026 CHEVROLET SILVERADO EV, 2026 GMC SIERRA EV

  An indicator light that does not illuminate may fail to warn the driver of an ESC system issue, increasing the risk of a crash.

  Unclassified

• Vehicle Recall · November 9, 2025

  Chrysler (FCA US, LLC)

  2023 JEEP WAGONEER, 2023 JEEP GRAND WAGONEER, 2024 JEEP GRAND WAGONEER, 2024 JEEP WAGONEER, 2025 JEEP WAGONEER, 2025 JEEP GRAND WAGONEER

  Detached trim pieces can create a road hazard for other vehicles, increasing the risk of a crash.

  Unclassified

• Vehicle Recall · November 9, 2025

  Ford Motor Company

  2024 FORD BRONCO

  A fuel leak in the presence of an ignition source increases the risk of a fire.

  Unclassified

• Vehicle Recall · November 9, 2025

  KTM North America, Inc.

  2023 HUSQVARNA SVARTPILEN 401, 2023 KTM 390 ADVENTURE, 2024 KTM 390 ADVENTURE

  Loss of drive power while riding increases the risk of a crash or injury.

  Unclassified

• Vehicle Recall · November 9, 2025

  Toyota Motor Engineering & Manufacturing

  2023 TOYOTA GR COROLLA, 2023 TOYOTA RAV4, 2023 TOYOTA RAV4 PRIME, 2023 TOYOTA HIGHLANDER, 2023 TOYOTA VENZA, 2023 TOYOTA CROWN, 2024 TOYOTA VENZA, 2024 TOYOTA CROWN, 2024 TOYOTA RAV4, 2024 TOYOTA GR C

  An instrument panel display that does not show critical information can increase the risk of a crash or injury.

  Unclassified

• Food Recall · November 8, 2025

  Pacific Seafood - Portland, LLC

  Pacific Seafood Raw Blackened Shrimp Peeled & Deveined Tail-Off, refrigerated, farm-raised. Net wt. per tray 8 oz (227 g). UPC 0 27241 44630 5. Ingredients: Shrimp (Shrimp, Water, Salt, Sodium trip

  Undeclared Sulfite. Shrimp may contain 3.4mg Sulfur Dioxide per serving and label does not declare Sulfite.

  Class III

• Food Recall · November 8, 2025

  ByHeart, INC.

  1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams; Cans sold in 1 pack, 2 packs, 4 packs, or 6 packs 2. ByHeart Whole Nutrition Infant Formula Anywhere Packs Single Serve Packet 17 grams

  Contaminated with Clostridium botulinum

  Class I

• Medical Device Recall · November 7, 2025

  Intuitive Surgical, Inc.

  Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System Model/Catalog Number: IS4000; IS4200; IS5000 Software Version: N/A Product Description: The da Vinc

  Due to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use. This test was supposed to be used to detect Universal Surgical Manipulator insertion axis ball screws that exhibit the symptoms of being bent and misaligned which is a precursor to potential ball screw fatigue failure/fraction

  Class II

• Medical Device Recall · November 7, 2025

  Rocket Medical Plc

  Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-18-SG Software Version: N/A Product Description: Chest tube manufactured from PVC, wi

  IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

  Class II

• Vehicle Recall · November 7, 2025

  Jaguar Land Rover North America, LLC

  2024 JAGUAR E-PACE

  A 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

• Medical Device Recall · November 7, 2025

  Rocket Medical Plc

  Brand Name: Rocket Product Name: Rocket 16Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54549-16-PK Software Version: N/A Product Description: Chest tube manufactured from PVC, with

  IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

  Class II

• Vehicle Recall · November 7, 2025

  Ford Motor Company

  2023 FORD BRONCO SPORT, 2024 FORD BRONCO SPORT

  A fuel leak in the presence of an ignition source, such as hot engine or exhaust components, can increase the risk of a fire.

  Unclassified

• Drug Recall · November 7, 2025

  Teva Pharmaceuticals USA, Inc

  Carton label: Testosterone Gel 1%, 2.5 grams per unit dose, CIII, 30 unit-dose packets, Rx only, Manufactured by: Actavis Laboratories, Inc, Salt Lake City, UT 84108, Distributed by: Actavis Pharma, I

  Defective Container - A defect in the side-seal which allows leakage of product.

  Class III

• Medical Device Recall · November 7, 2025

  Rocket Medical Plc

  Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-12-SG Software Version: N/A Product Description: Chest tube manufactured from PVC, wi

  IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

  Class II

• Vehicle Recall · November 7, 2025

  Daimler Vans USA, LLC

  2023 MERCEDES-BENZ METRIS

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

  Unclassified

• Food Recall · November 7, 2025

  Anthony's BBQ

  Anthony's Barbecue & Dip-It Sauce, 15 oz. (425g) glass bottle, UPC 6 89076 62272 1. Anthony's BBQ Sauce PO Box 3239 Harbor, OR 97415. The ingredients statement on the recalled bottle is declared as "

  Undeclared allergen (fish). Anthony's Barbecue & Dip-It Sauce label does not declare Worcestershire (Anchovy).

  Class I

• Food Recall · November 7, 2025

  Costco Wholesale Corporation

  Costco Item# 11444 Kirkland Signature Chicken Sandwich with Caesar Salad, refrigerated, packaged in clear plastic clamshell container. The net weight varies as it is sold by weight. This product cont

  The 3oz. sealed packet of Caesar Dressing in Costco Chicken Sandwich w/ Caesar Salad may contain plastic material.

  Class II

• Food Recall · November 7, 2025

  Costco Wholesale Corporation

  Costco Item# 19927 Kirkland Signature Caesar Salad, refrigerated, packaged in clear plastic clamshell container. The net weight varies as it is sold by weight. This product contains 3oz. sealed packet

  The 3oz. sealed packet of Caesar Dressing in Costco Caesar Salad may contain plastic material.

  Class II

• Medical Device Recall · November 7, 2025

  Beckman Coulter, Inc.

  Access 2 Reaction Vessels, individual, disposable, plastic tubes used to process patient, quality control and calibration samples on the Access 2 Immunoassay system, Catalog Number 81901

  It has been determined that certain lots of Access 2 Reaction Vessels may contain manufacturing deformities. The bottom (round end) of the Reaction Vessel may have a small protrusion or hair like deformity. This could cause causing instrument errors (e.g., pipetting, rake, wash carousel errors) that could delay patient results.

  Class II

• Medical Device Recall · November 7, 2025

  Rocket Medical Plc

  Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54549-20-PK Software Version: N/A Product Description: Chest tube manufactured from PVC, with

  IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

  Class II

• Medical Device Recall · November 7, 2025

  Rocket Medical Plc

  Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-18-PK Software Version: N/A Product Description: Chest tube manufactured from PVC, with

  IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

  Class II

• Medical Device Recall · November 7, 2025

  Rocket Medical Plc

  Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-12-PK Product Description: Chest tube manufactured from PVC, with fenestrations and a bar

  IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

  Class II

• Medical Device Recall · November 6, 2025

  CareFusion 303, Inc.

  BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System with Guardrails" Suite MX is a modular infusion pump and monitoring system for the continuous or intermittent a

  Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital networks. This issue only affects the Interoperability workflow for devices with a DST invalid timestamp, impacting connectivity of the PCU to the hospital network

  Class II

• Medical Device Recall · November 6, 2025

  C.R. Bard Inc

  BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826

  Labeling discrepancy; Ureteral stent actual size may not match the actual product label.

  Class II

• Medical Device Recall · November 6, 2025

  Bard Peripheral Vascular Inc

  Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,

  Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that erroneously show catheter in sharp position when catheter is in blunt position, which may lead users to believe device is not yet in pleural or peritoneal space when it is, may cause discomfort, delay to treatment, injury to internal organs or vessels.

  Class II

• Consumer Product Recall · November 6, 2025

  Shanghai Siwu Jidan Shangmao Youxian Gongsi, dbaWYBITNY, of China

  Children's WYBITNY Bed Rails

  The recalled bed rails violate the mandatory standard for children's portable bed rails because, when installed adjacent to the bed, the child can become entrapped in the enclosed openings, the openings on the side of the mattress, and the openings on top of the mattress, posing a risk of serious injury or death due to entrapment.

  Unclassified

• Consumer Product Recall · November 6, 2025

  Peloton Interactive Inc., of New York

  Peloton Original Series Bike+ Model PL02

  The bike's seat post assembly can break during use, posing fall and injury hazards to the user.

  Unclassified

• Medical Device Recall · November 6, 2025

  C.R. Bard Inc

  BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630

  Labeling discrepancy; Ureteral stent actual size may not match the actual product label.

  Class II

• Medical Device Recall · November 6, 2025

  PATH

  MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe (P/N 8-69-41100)

  Following a component change in the DPOAE probe (speaker replacement), technical distortions may occur at high stimulus levels combined with unusually low OAE amplitude acceptance thresholds. These distortions can mimic true DPOAE responses and may result in a false PASS outcome.

  Class II

• Consumer Product Recall · November 6, 2025

  Ruiyewenhuachuanboshenzhenyouxiangongsi, dba Neaude, of China

  Neaude Adult Portable Bed Rails

  The recalled bed rails violate the mandatory standard for adult portable bed rails, posing a serious entrapment hazard and risk of death by asphyxiation. 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. In addition, the bed rails do not have the required warning labels.

  Unclassified

• Food Recall · November 6, 2025

  VENTURA FOODS LLC

  Publix Deli Carolina-Style Mustard BBQ Sauce; 96- 2OZ NET WT: 12 LB SKU: 10 026700 16964 6

  foreign objects (black plastic planting material) in granulated onion

  Class II