Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,094 recalls have been distributed to Ohio in the last 12 months.
Showing 17301–17320 of 55,415 recalls
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to...
The Issue: Retrospective reporting for the release of Technical Bulletin IMP-2643 AIC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cellex qSARS-Cov-2 Antigen Rapid Test Recalled by Cellex Due to The kit does...
The Issue: The kit does not have an emergency use authorization (EUA).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic pulsed doppler imaging system - Product Usage: intended for...
The Issue: Arietta 850 software version 4.0.0., 4.0.1, and 4.0.2 has an error in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyWay Walker Chassis - Product Usage: is intended for use Recalled by James...
The Issue: Due to a failure of the welds, the casters detached from the rear legs of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE DIAGNOSTICS FenomPro SN ***** - Product Usage: a portable Recalled by...
The Issue: Erroneously high FeNO levels which may contribute to premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Treatment Delivery System - Product Usage: indicated for...
The Issue: The set screws that connect the Standard Treatment Couch linkage arm to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System - Product Usage: developed for...
The Issue: Siemens has become aware of a potential issue in which the imaging system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRAVO PH CAPS DELIVERY DEV5-PK Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CF Delivery Dev Caps Bravo x5 Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to There is a...
The Issue: There is a potential for tube trays to leak which could potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Their is a potential that...
The Issue: Their is a potential that Video Processor/Illuminators may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: Medtronic HeartWare HVAD System Instructions for Use (IFU) and Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe Expected Alarm Duration. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe HVAD Controller Connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrolit Ponche/Fruit Punch Recalled by Laboratorios Pisa Sa De Cv Due to...
The Issue: Product contains undeclared FD&C Red No. 40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: tastebuds Taco Dip Recalled by J & J Distributing Company Due to Potential...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: tastebuds Taco Platter Recalled by J & J Distributing Company Due to...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Haug Fresh Mini 7 Layer Dip Tray Recalled by J & J Distributing Company Due...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taco Dip [Kwik Trip] Recalled by J & J Distributing Company Due to Potential...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fresh Thyme Taco Dip Recalled by J & J Distributing Company Due to Potential...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.