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. 2,580 recalls have been distributed to Ohio in the last 12 months.
Showing 25841–25860 of 55,415 recalls
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS...
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number: Recalled by Orthofix Srl Due to As a result of...
The Issue: As a result of complaint investigations it was determined that batches of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Millville Maple & Brown Sugar Instant Oatmeal 15.1 oz. 10 Recalled by Aldi...
The Issue: Complaints of insects in product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prevacid 24HR (Lansoprazole) delayed-release capsules Recalled by...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PCEA Kit ASV Yellow Stripe Microbore Recalled by Becton Dickinson & Company...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCEA ASV Yellow Microbore Recalled by Becton Dickinson & Company Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TB Series Bipolar Pacing Leads Recalled by Oscor, Inc. Due to During the use...
The Issue: During the use of some TB - Temporary Bipolar Pacing Leads, featuring the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation...
The Issue: An incorrect display of the Biopsy Depth Gauge graphical representation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer: In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime. In vitro diagnostic testing of clinical...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 635 Biliary Stent 4mm x 80mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.