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. 1,904 recalls have been distributed to Ohio in the last 12 months.
Showing 29621–29640 of 55,415 recalls
Recalled Item: Rhubarb Pie Baked whole pies & frozen pies Recalled by Stevens Family Bakery...
The Issue: Product contains undeclared milk - label failed to include the components of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...
The Issue: Superpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bean Boy Coffee Dark Chocolate Covered Espresso Beans Recalled by Pacific...
The Issue: Pacific Rim Distribution Inc., dba Bean Boy Coffee is voluntarily recalling...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...
The Issue: Device may potentially be compromised by water in end user packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...
The Issue: Device may potentially be compromised by water in end user packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bupPROPion HCL Extended-Release Tablets Recalled by Mylan Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: Mylan Pharmaceuticals Inc. is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Handicare C Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handicare P600 Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH800 Recalled by Beckman Coulter Inc. Due to The shield for the...
The Issue: The shield for the Single-Tube Station on the DxH instrument may interfere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden Classic 38 Sphere Daily Wear Soft contact Recalled by Alden Optical...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Daily Wear Soft contact Recalled by Alden Optical Due to Contact...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP59 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP49 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH600 Recalled by Beckman Coulter Inc. Due to The shield for the...
The Issue: The shield for the Single-Tube Station on the DxH instrument may interfere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP49 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.