Safety Recalls

17,560 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

Showing 4,851–4,900 of 17,560

• Food Recall · November 13, 2025

  MEI YU CHENG DA TRADING INC

  DADI NONGFU DRIED SALT CHILLI VEGETABLE(S); Ingredients: Radish, chili, roasted sesame, prickly ash, edible salt, soybean oil, edible vinegar, white granulated sugar, spices, food additives (sodium gl

  Products contain banned sweetener: cyclamates.

  Class III

• Vehicle Recall · November 13, 2025

  Grand Design RV, LLC

  2023 GRAND DESIGN SOLITUDE, 2023 GRAND DESIGN MOMENTUM

  A propane leak in the presence of an ignition source can increase the risk of a fire.

  Unclassified

• Vehicle Recall · November 13, 2025

  Honda (American Honda Motor Co.)

  2023 HONDA ACCORD HYBRID, 2024 HONDA ACCORD HYBRID, 2025 HONDA ACCORD HYBRID

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

  Unclassified

• Medical Device Recall · November 13, 2025

  Abbott Laboratories

  Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20

  Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction. The reason for the recall is potential performance issues found in the Alinity ci-series System software versions 3.6.1. and lower that could lead to erroneous results for multiple analytes. The issue was identified by Abbott during the internal testing of complaint investigations.

  Class II

• Food Recall · November 13, 2025

  MEI YU CHENG DA TRADING INC

  Olive Skewers individually wrapped and packaged in clear plastic bag; 500g; INGREDIENTS: Olive, edible salt, white sugar, monosodium glutamate, licorice, cloves, food additives (citric acid, DL malic

  Products contain banned sweetener: cyclamates.

  Class III

• Consumer Product Recall · November 13, 2025

  Shantou Chenghai Xingzigu Toy Industry Co., Ltd., of China

  Bettina Doll Set with Magic Light Unicorn

  The doll sets violate the mandatory standard for toys because the battery compartment of the unicorn 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 · November 13, 2025

  Trek Bicycle Corporation, of Waterloo, Wisconsin

  Trek and Electra-branded Bicycles with Coaster Brakes and Replacement Rear Wheels with Coaster Brakes

  The coaster brakes can fail to engage, resulting in the rider losing control, posing a crash hazard.

  Unclassified

• Consumer Product Recall · November 13, 2025

  Belkin International Inc., of El Segundo, California

  Portable Power Banks and Wireless Charging Stands

  The lithium-ion battery in the power banks and charging stands can overheat, posing fire and burn hazards to consumers.

  Unclassified

• Consumer Product Recall · November 13, 2025

  Mobi Games, Inc. of Canada

  Zippee Activity Toys

  The recalled silicone activity toys contain spherical ends that can reach the back of the throat, posing a serious choking hazard to children.

  Unclassified

• Consumer Product Recall · November 13, 2025

  Changzhoulongzhiyuedianzishangwuyouxiangongsi dba Zigjoy-US, of China

  Zigjoy Toddler Sleep Sacks with Feet

  The recalled sleep sacks violate the mandatory flammability standard for children's sleepwear, posing a burn hazard and risk of serious injury or death to children.

  Unclassified

• Food Recall · November 13, 2025

  Jeni's Splendid Ice Creams LLC

  Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton with Item UPC: 850060644122, packed 8 retail cartons per case with Case UPC: 1085006

  Undeclared allergens - wheat and soy

  Class II

• Food Recall · November 13, 2025

  American Nuts, LLC

  Dry Roasted Baking Macadamia Nuts, Unsalted Halves Ideal for Baking, Cooking, Salads or Ice Cream; NET WT 20 OZ (1 LB 4 OZ) 567g UPC: 8 60011 44301 8

  Potential Salmonella contamination.

  Class I

• Food Recall · November 13, 2025

  Meijer Inc

  Meijer Steam Distilled Water, 128 FL OZ (1 GAL) 3.78L, packaged in a plastic jug with red plastic lid, UPC 041250841197, Dist. By Meijer Distribution, Inc. Grand Rapids, MI 49544, packed 4 per case

  Floating black foreign substance in the product

  Class II

• Vehicle Recall · November 12, 2025

  Volkswagen Group of America, Inc.

  2025 AUDI Q7, 2025 AUDI Q8

  A seat belt that is missing a rivet may not properly restrain an occupant during a crash, increasing the risk of injury.

  Unclassified

• Medical Device Recall · November 12, 2025

  Cardinal Health 200, LLC

  ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Non-sterile; CT5502T ChemoPlus Full Coverage Gown, Closed Back, Regular/Medium, Med

  Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.

  Class II

• Medical Device Recall · November 12, 2025

  Remel, Inc

  1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

  Products may contain contamination, which may result in a darker or brown media color.

  Class II

• Medical Device Recall · November 12, 2025

  Howmedica Osteonics Corp.

  The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR) light-emitting diodes (LEDs) as well as an electronics control unit fo

  When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.

  Class II

• Food Recall · November 12, 2025

  Stuffed Foods LLC

  Stuffed Foods brand Cacio e Pepe Arancini; KEEP FROZEN; For institutional use only; Ready-to-cook; Cook to internal temp. of 165oF; Case pack: 3/3 lbs; Net Weight: 9lbs; UPC 00819985020787

  Undeclared Soy Protein Concentrate

  Class I

• Food Recall · November 12, 2025

  Genepro Protein, Inc.

  Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable mylar bag, UPC 850053365126, Manufactured For: Genepro Protein, Inc. 15000 Weston Pa

  Product is mislabeled - the labeling contains incorrect ingredient information and fails to declare milk as an allergen

  Class I

• Drug Recall · November 12, 2025

  Medical Products Laboratories, Inc.

  Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01

  Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis

  Class II

• Food Recall · November 12, 2025

  Santos Agency Inc.

  Brass Langri Cookware Sticker label: 14

  Potential contamination due to leachable lead.

  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: LLOG1000-15.

  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. 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 Inner Sheath, for 26 Fr. Outer Sheath. Model No. A22040A. 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 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 11, 2025

  AVID Medical, Inc.

  Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08

  Devices are not suitable for organ transplant.

  Class I

• Medical Device Recall · November 11, 2025

  Olympus Corporation of the Americas

  Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological 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.; Model No. A22042A. 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. 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

  Olympus Corporation of the Americas

  Olympus Resection Sheath, 28 Fr.; Model No. A22043A. 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 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

• Medical Device Recall · November 11, 2025

  Medline Industries, LP

  DEXLOCK Achilles Repair Implant Kits, MAKT4520

  There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit and drill guide may prolong the surgical procedure.

  Class II

• Medical Device Recall · November 11, 2025

  Olympus Corporation of the Americas

  Olympus Inner Sheath 21 Fr. Model No. A2660T. 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 Sheath, 10 Fr. Model No. A37004A. 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; Model No. A2666. Resection sheath for urologic applications.

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

  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

• Medical Device Recall · November 11, 2025

  Olympus Corporation of the Americas

  Olympus Resection Sheath. Model No. A22014A and A22014T. 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 Inner Sheath. Model No. A2642. 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, 24 Fr; Model No. A22041A. 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, Long; Model No. WA22017T. Inner sheath for urological and gynecological 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

• 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

• 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. A2641. 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, 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

• 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, 28 Fr. with Deflecting Obturator. Model No. A22043T. 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, Long; Model No. WA22017A. Inner sheath for urological and gynecological applications.

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

  Class II

• 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