Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,501–7,550 of 15,271
- Unclassified
Consumer Product Recall · March 13, 2025
Gerolsteiner Brunnen GmbH & Co. KG, of Germany
Gerolsteiner 750ml Sparkling Water BottlesThe recalled water bottles can crack, causing a laceration hazard.
- Class II
Food Recall · March 13, 2025
SeaBear Smokedhouse Alehouse Clam Chowder is packaged in retort pouch, net wt. 12-oz., UPC 0 34507 07021 1. Case label, item 60104, Alehouse Chowder 12/CS.Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
- Unclassified
Consumer Product Recall · March 13, 2025
Shenzhenshiyaxinrankejiyouxiangongsi, dba Blissful-Time, of China
Onasti Toddler Tower StoolsThe stools can collapse or tip over while in use, posing serious fall and injury hazards to children.
- Unclassified
Consumer Product Recall · March 13, 2025
Yiwushihengchuansanyeyouxiangongsi, dba HabiLife Direct, of China
Retractable Safety GatesThe recalled gates violate the federal safety regulations for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and the floor, posing a risk of serious injury or death due to entrapment hazard.
- Class II
Drug Recall · March 13, 2025
Glenmark Pharmaceuticals Inc., USA
Cetirizine Hydrochloride Tablets, USP, 10mg, 365-count packs, Rx Only, Manufactured for: Glenmark Therapeutics Inc., Distributed by: Amazon. NDC# 72657-129-35CGMP Deviations
- Class II
Food Recall · March 13, 2025
COFFEE ROASTERS Our Family TRAVERSE CITY CHERRY ARTIFICIALLY FLAVORED DECAF LIGHT ROAST GROUND COFFEE NET WT 12 OZ (340g) UPC 0 70253 11080 1 DISTRIBUTED BY THE SPARTANNASH COMPANY GRAND RAPIDS, MI 49Mislabeling. A portion of the production of Our Family Traverse City Ground Coffee was mislabeled as decaffeinate.
- Class II
Food Recall · March 13, 2025
SeaBear Smokedhouse Salmon Chowder is packaged in flexible retort pouch, net wt. 12-oz., UPC 0 34507 07001 3. Case label: Item 60077 Salmon Chowder 12/12oz, SeaBear/G&D Anacortes, WA.Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
- Unclassified
Consumer Product Recall · March 13, 2025
Chews Life, of Grand Rapids, Michigan
Silicone Rosary and Decade teethersPart of the teethers' safety snap clasp can detach, posing a choking hazard.
- Unclassified
Consumer Product Recall · March 13, 2025
Meijer Distribution Inc., of Grand Rapids, Michigan
Konwin Desktop HeatersThe heater's fan can fail to turn on and cause the unit to overheat and ignite, posing fire and burn hazards.
- Unclassified
Consumer Product Recall · March 13, 2025
BMC Switzerland AG, of Switzerland
BMC-branded Kaius 01 bicycles and framesetsThe fork steerer tube on the recalled bicycles and framesets can crack, break, or separate during use, posing a fall hazard.
- Class I
Medical Device Recall · March 12, 2025
Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases betweenThe potential for cracks forming in the breathing circuit hose.
- Class II
Food Recall · March 12, 2025
Julie's Gorditas De Nata; Ingredients: Flour, Vegetable Oil, Sugar, Baking Soda, Milk, Sour Cream, Butter, Cream Of Milk, Cinnamon, Vanilla; Net Wt. 16.75 OZ UPC# 0 00202 12018 6undeclared allergen ingredient (wheat) on product label for flour Gorditas.
- Class II
Drug Recall · March 12, 2025
Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc Oxide, 3 FL OZ/ 85 mL per bottle, Made in USA for Erin's Faces, Millburn, NO 07041. NDC: 73369-1401-1cGMP deviations
- Class I
Medical Device Recall · March 12, 2025
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 Software Version: Not applicable Product Description: Accessory for conducting medicalThe potential for cracks forming in the breathing circuit hose.
- Class II
Medical Device Recall · March 12, 2025
Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version: n/a Component: n/aIdentified faulty cartridges. If such a faulty cartridge is used for sample testing, false test results could occur.
- Class I
Medical Device Recall · March 12, 2025
Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: TA-06-0001 Product Description: Common Name: Diagnostic intravascular catheter Description: The NoDue to manufacturing issues there is a potential for the catheter sheath to detach.
- Class I
Medical Device Recall · March 12, 2025
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 Software Version: Not applicable Product Description: Accessory for conducting medicalThe potential for cracks forming in the breathing circuit hose.
- Class II
Drug Recall · March 12, 2025
Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%), Packaged as a) 6 fl. oz. (177.4 mL), UPC 7 35786 01528 2; b) 0.33 OZ (9.45g), UPC 8 42944 10223 1; Distributed by Alchemee, LLC, Santa MonicChemical contamination: Presence of benzene
- Class II
Drug Recall · March 12, 2025
Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%), 0.33 oz. (9.45 g), Distributed by Alchemee LLC, Santa Monica, CA 90401, Made in the USA, UPC 7 35786 01921 1, UPC 8 42944 10223 1, and also paChemical contamination: Presence of benzene
- Class I
Medical Device Recall · March 12, 2025
Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between anThe potential for cracks forming in the breathing circuit hose.
- Class II
Food Recall · March 12, 2025
emd Oysterettes (oyster crackers in polypropylene film). 0.75 oz. Packed for and Distributed by emd, Detroit, MI 48212.Foreign object (metal)
- Class I
Medical Device Recall · March 12, 2025
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model/Catalog Number: MP02752 Software Version: Not applicable Product Description: Accessory for conducting medicThe potential for cracks forming in the breathing circuit hose.
- Class I
Medical Device Recall · March 12, 2025
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medicalThe potential for cracks forming in the breathing circuit hose.
- Unclassified
Vehicle Recall · March 12, 2025
Volkswagen Group of America, Inc.
2023 VOLKSWAGEN ID.4, 2024 VOLKSWAGEN ID.4A vehicle fire while parked or driving can increase the risk of injury.
- Unclassified
Vehicle Recall · March 12, 2025
Volkswagen Group of America, Inc.
2026 VOLKSWAGEN ATLASIncorrect wheel bolts can allow a wheel to detach from the vehicle, increasing the risk of a crash.
- Class II
Food Recall · March 12, 2025
Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months. UPC 1 91907-99314 1. Distributed by Target Corporation, Minneapolis, MN 55403. Product of Colombiaelevated level of lead
- Class I
Medical Device Recall · March 12, 2025
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medicaThe potential for cracks forming in the breathing circuit hose.