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. 2,786 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,786 in last 12 months

Showing 52015220 of 55,415 recalls

Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Libre 3 Sensors Recalled by Abbott Diabetes Care, Inc. Due to...

The Issue: Users of the FreeStyle Libre 3 sensors reported situations where they were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Precision Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Precision Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Cardinal Health 200, LLC

Recalled Item: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube with Anti- Valve...

The Issue: The firm received reports of breakage in the Anti- Valve (ARV) due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Cardinal Health 200, LLC

Recalled Item: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube Recalled by Cardinal...

The Issue: The firm received reports of breakage in the Anti- Valve (ARV) due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 24, 2024· B. Braun Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Presence of Particulate Matter

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 23, 2024· FDC Limited

Recalled Item: Ciprofloxacin ophthalmic solution USP Recalled by FDC Limited Due to...

The Issue: Defective container: unable to get the solution out of the bottle as the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2024· Unomedical A/S

Recalled Item: VariSoft Infusion Set Recalled by Unomedical A/S Due to Specific VariSoftTM...

The Issue: Specific VariSoftTM Infusion Sets were packaged using incorrect secondary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 22, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Glenmark Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 20, 2024· Izzio Artisan Bakery, LLC

Recalled Item: Izzio Everything Sourdough. Single 24oz loaf packaged into plastic bag....

The Issue: Potential foreign material - plastic

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 20, 2024· Izzio Artisan Bakery, LLC

Recalled Item: Aldi Mixed Sourdough loaf. A single 24oz loaf packaged into plastic bag...

The Issue: Potential foreign material - plastic

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund