Home / Recalls
Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
April 16, 2025Medical DevicesFDA
Tornier S.A.S. recalls stryker Blueprint Mixed Reality Coracoid Clamp, Catalog Number MRUE202, packaged in stryker Blueprint Mixed Reality Inst
Hazard: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
April 16, 2025Medical DevicesFDA
Tornier S.A.S. recalls stryker Blueprint Mixed Reality Glenoid Digitizer, Catalog Number MRUE201, packaged in stryker Blueprint Mixed Reality I
Hazard: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
April 16, 2025Medical DevicesFDA
Tornier S.A.S. recalls stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless Steel, Catalog Number MRUE200, packaged in str
Hazard: Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
April 16, 2025Medical DevicesFDA
Omnicell, Inc. recalls IVX Station Reconstitution Transfer Set. Model Number: 298921215. Packaging: 1 set per White Tyvek Pouch, 5 Tyvek Pouche
Hazard: IVX Station Reconstitution Transfer Sets were shipped in advance of the IVX Station upgrade and not intended for clinical use but are engineering devices intended for use during set up and system calibration. The items were not shipped in a validated packing configuration and sterility cannot be ensured.
April 16, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT, Model Number: MJ18004V2; 2) MJ BANDAGE HYDROCOL
Hazard: There is a potential for the sterility of the device to be compromised.
April 16, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Wayson Hydrocolloid Models: 1) Model Number: CUR5103, DBD-BNDG,WTRPRF,HYDRCLLD,CLR,2.36X3.93", 2) Model Number: MJ1800
Hazard: There is a potential for the sterility of the device to be compromised.
April 16, 2025Medical DevicesFDA
Beckman Coulter, Inc. recalls DxI 9000 Access Immunoassay Analyzer, catalog number C11137 in vitro diagnostic device used for the quantitative, se
Hazard: Ground screws on Dxl 9000 PCB boards may cause electric shorts, leading to smoke and potentially delaying patient results. Smoke also poses a hazard to equipment and users.
April 16, 2025Medical DevicesFDA
BioFire Diagnostics, LLC recalls FilmArra Pneumonia Panel plus (Pneumoplus), REF: RFIT-LBL-0374
Hazard: Increased risk of control failures and false negative test results with multiplexed nucleic acid test.
April 16, 2025Medical DevicesFDA
Qapel Medical Inc. recalls Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072 Aspira
Hazard: Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur.
April 16, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical convenience kits labeled as: 1) NEONATAL INTUBATION TRAY, REF ACC010371C; 2) NEWBORN RESUSCITATION
Hazard: Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.
April 16, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CPB ADJUNCT PACK, DR. C
Hazard: Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
April 16, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF
Hazard: Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
April 16, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: TOL DR R PACK
Hazard: Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
April 16, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARD
Hazard: Medline medical procedure kits, containing Medtronic Aortic Root Cannula
April 16, 2025Food & BeverageFDA
Victor Packing Inc. recalls Dried Cranberries (21.75 lb/case; 300 - 1.16 oz packages/case)
Hazard: Misbranded - label states 2g total carbohydrates instead of 27g
April 16, 2025Food & BeverageFDA
C.H. Guenther & Son LLC recalls 365 Whole Foods Market Small Bites Macaroni & Cheese. Net Wt 8.5 oz (240g) Keep Frozen. UPC 99482499709. Distributed
Hazard: Undeclared allergen (eggs) and pork
April 16, 2025Food & BeverageFDA
The Truck Farm, LLC recalls Desert Farms Jalapeno Mustard. Caution to refrigerate after opening. The shelf life is 2 years after the date of manufac
Hazard: The product is in violation for not having an approved filed process and for not having monitoring records.
April 16, 2025Food & BeverageFDA
Harvey Investments LLC / The Baking Group recalls Brioche Bread Loaf and Hamburger buns packaged in brown box and labeled as follows: 1. Ben E. Keith Co. Dense Brioche
Hazard: Undeclared allergens (soy, milk) and Yellow #5
April 16, 2025Food & BeverageFDA
OLD WORLD SPICES & SEASONING, INC recalls Lillie's Q Buffalo Wing Sauce. Net wt. 13.5 oz, UPC 810069510972, Case label: Lillie's Q Buffalo Wing Sauce, Item # FGLO
Hazard: Undeclared allergen (milk not listed as sub ingredient of butter). Milk also not listed in 'Contains' statement.
April 16, 2025Food & BeverageFDA
MTN OPS, LLC recalls MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement, 60 Capsule Bottle (30 Serving). Manufactured exclusively f
Hazard: Undeclared soy flour
April 16, 2025Food & BeverageFDA
AGRI-MARK INC recalls Cabot Creamery 8oz Extra Creamy Premium Butter, Sea Salted. Packaged as (2) 4oz sticks in cardboard shells; UPC: 0 78354
Hazard: Product contaminated with elevated levels of coliform.
April 16, 2025Food & BeverageFDA
Red Shell Foods, Inc. recalls Teriyaki Sauce, Red Shell branded. Ingredients: Soy sauce(water, soybeans, wheat, salt, sodium benzoate), water, sugar,
Hazard: Shelf stable Teriyaki sauce showing signs of micro growth (bubbling) and swelling containers.
April 16, 2025Food & BeverageFDA
Kedake Inc recalls Las Ollas Botana Mix snack, 2lbs, item #1516, # 1056, UPC# 880342001855
Hazard: Undeclared Sesame, Soy, Wheat, Yellow No. 5, Yellow No. 6, and Red No. 6.
April 16, 2025Food & BeverageFDA
Dr. Praeger's Sensible Foods Inc. recalls Dr. Praeger s California Veggie Fries 8oz,
Hazard: Undeclared Allergen (Soy)
April 16, 2025DrugsFDA
Zydus Pharmaceuticals (USA) Inc recalls chlorproMAZINE Hydrochloride Tablets, USP 10 mg, Rx Only, 100 Tablets bottles, Manufactured by: Zydus Lifesciences Ltd.,
Hazard: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit
April 16, 2025DrugsFDA
Alchemee, LLC recalls Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%), Packaged as a) 6 fl. oz. (177.4 mL), UPC 7 35786 01528 2; b)
Hazard: Chemical contamination: Presence of benzene
April 16, 2025DrugsFDA
Alchemee, LLC recalls Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%), 0.33 oz. (9.45 g), Distributed by Alchemee LLC, Santa Monica, C
Hazard: Chemical contamination: Presence of benzene
April 16, 2025DrugsFDA
Somerset Therapeutics Private Limited recalls Haloperidol Decanoate Injection, 100 mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured for: Somerset Therapeutics, LLC,
Hazard: Lack of Assurance of Sterility: Media fill with bacterial contamination
April 16, 2025DrugsFDA
Somerset Therapeutics Private Limited recalls Haloperidol Decanoate Injection 100mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured by: Somerset Therapeutics Limited,
Hazard: Lack of Assurance of Sterility: Media fill with bacterial contamination
April 16, 2025DrugsFDA
Somerset Therapeutics Private Limited recalls Haloperidol Decanoate Injection 50mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured by: Somerset Therapeutics Limited,
Hazard: Lack of Assurance of Sterility: Media fill with bacterial contamination