Back to recall look-up

Recall archive

94,914 stored notices, from Jun 20, 2012 to Oct 21, 2026.

32,165 recalls · page 497 of 1341

Meat & poultry

Reported Aug 24, 2021

Willow Tree Poultry Farm Recalls Chicken Salad and Dip Products Due to Possible Foreign Matter Contamination

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Willow Tree Poultry Farm, Inc.

USDA FSIS

Consumer products

Reported Aug 19, 2021

John Deere Recalls Compact Utility Tractors Due to Risk of Injury (Recall Alert)

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Deere & Company

CPSC

Consumer products

Reported Aug 19, 2021

Infant Bath Seats Recalled Due to Drowning Hazard; Imported by Frieyss and Sold Exclusively on Amazon.com (Recall Alert)

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Qingdao Ruizexin Electronic Technology Co. Ltd.

CPSC

Food

Reported Aug 18, 2021

5000 Years Foods SLICED CABBAGE KIMCHI in 5GAL plastic tubs, and 128 oz, 64 oz, 32 oz, & 16 oz glass jars

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

5000 Years Foods, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 18, 2021

Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro diagnostic use in blood donor screening,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Advance Dx 100 Blood Collection Card Quantity 25 REF CMT01 Advance Dx 100 Blood Collection Card and Foil Bags Quantity…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Advance Dx, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Aug 18, 2021

Sulfamethoxazole and Trimethoprim Tablets, USP, 800mg/160mg Double Strength, 500 Tablets, Rx Only, Distributed by:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Aurobindo Pharma USA Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 18, 2021

TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 15 cm; TJC3513…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

ACCESS SARS-CoV-2 Antigen , REF: C68668, IVD, Rx only, UDI: (01) 15099590742713;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Kaluza C Flow Cytometry Software Versions: 1.0*, 1.1.1 and 1.1.2 Kits: C10574 - Kaluza C Single Perpetual License…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

FilmArray Blood Culture Identification (BCID) Panel Product Pouch Label: FilmArray BCID Panel Part No: RFIT-ASY-0126…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Alaris Infusion Pump Module, Model 8100, serviced/repaired by Biomedical Equipment Service Co. (BMES) with an impacted…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

BioMedical Equipment Service Co. (BMES)

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

ETEST IMIPENEM RELEBACTAM. in vitro diagnostic

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

MYLA software. Used to manage microbiology test workflow from the reception of requests to the transmission of results…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Arcos Modular Revision Hip System Standard Cone Prox Body, Size A, 50 MM Item Number: 11-301300

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet, Inc.

16 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carl Zeiss Meditec, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Cordis SABER PTA Balloon Dilation Catheter, 4F, REF 48004010X

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Covidien Sonicision Reusable Generator-converts electrical power from the battery pack to ultrasonic energy to drive…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien LLC

FDA (openFDA device enforcement)

Food

Reported Aug 18, 2021

Dark Chocolate Malt Balls in plastic container; 9 oz./ 255g UPC: 6 5143370179 0 Packed on the same equipment as…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

DSD Merchandisers, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 18, 2021

The device is a 25-gauge infusion line that is part of 25-gauge surgical pack labeled TDC Vitrectomy Pack VGPC 25g,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dutch Ophthalmic USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 18, 2021

Edwards PediaSat Oximetry Catheter Kit, REF: XT3515KTP, Exterior Diameter 5.5F (1.83 mm), Usable Length 15 cm, Number…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Aug 18, 2021

Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use Vial, Rx only, Marketed by: Lilly USA, LLC,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Eli Lilly & Company

FDA (openFDA drug enforcement)

Medical devices

Reported Aug 18, 2021

Exactech BIOLOX delta Femoral Head, 36m O.D., REF 170-36-00. Hip prosthesis component.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Exactech, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

RecallNow is not a government agency. Every notice above is published by the FDA, USDA FSIS, or CPSC and links back to its source. Back to the look-up