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 25121–25140 of 55,415 recalls
Recalled Item: LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS Recalled by Torrent...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS Recalled by Torrent...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOSARTAN POTASSIUM TABLETS Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olmesartan Medoxomil and Hydrochlorothiazide Tablets Recalled by Teva...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...
The Issue: A software update is being issued to correct multiple issues identified in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Cincinnati Sub-Zero...
The Issue: Evidence supports that when customers performed a fuse replacement as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...
The Issue: The kits may contain the incorrect number of components or the kits may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...
The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RXBAR: Chocolate Hazelnut Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...
The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RXBAR: 14-Bar Variety Pack (Chocolate Chip and Chocolate Sea Salt) Recalled...
The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RXBAR: Coffee Chocolate Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...
The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RXBAR: Chocolate Chip Recalled by CHICAGO BAR COMPANY LLC RXBAR Due to...
The Issue: Chicago Bar Company LLC d/b/a RXBAR is voluntary recalling certain varieties...
Recommended Action: Do not consume. Return to store for a refund or discard.