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.

55,415 total recalls
2,580 in last 12 months

Showing 2964129660 of 55,415 recalls

Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP54 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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beaver-Visitec International Inc.

Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...

The Issue: The protective shield was retracted, and the blade was exposed.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP54 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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: Alden HP59 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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

Recalled Item: ASTERA Multifocal Toric 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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Recalled by Beckman Coulter Inc. Due to 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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Medtronic Inc.

Recalled Item: Everflex Self-Expanding Peripheral Stent with Entrust Delivery System...

The Issue: Stent length on the label may not match the length of the stent itself.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Volcano Corporation

Recalled Item: Volcano Imaging System s5i Recalled by Volcano Corporation Due to On certain...

The Issue: On certain Impacted Systems, an unexpected Microsoft Windows Security dialog...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Alden Optical

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.

Class II — Potential Health HazardOngoing
DrugNovember 3, 2017· Mylan Pharmaceuticals Inc.

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.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 3, 2017· Handicare Usa Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2017· Handicare Usa Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2017· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: NeoBase Succinylacetone Assay Solution Recalled by PerkinElmer Life and...

The Issue: There is a potential for leaking vials for certain lot numbers where, if...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2017· Pro-Med Instruments Gmbh

Recalled Item: pmi Recalled by Pro-Med Instruments Gmbh Due to The firm received reports of...

The Issue: The firm received reports of two breakages of the pin tips which occurred...

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

Class II — Potential Health HazardOngoing
FoodNovember 2, 2017· Gourmet International Inc.

Recalled Item: Premio Strawberry Pralinati Recalled by Gourmet International Inc. Due to...

The Issue: Gourmet International Inc. is initiating a voluntary recall of cookie...

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

Class III — Low RiskOngoing
Refund
FoodNovember 1, 2017· doTERRA International, LLC

Recalled Item: Slim & Sassy¿ TrimShake Vanilla Recalled by doTERRA International, LLC Due...

The Issue: doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake -...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch Recalled by Aurora...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Coffee beans packaged in Bulk 4 oz. Plastic Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· doTERRA International, LLC

Recalled Item: Slim & Sassy¿ TrimShake Chocolate Recalled by doTERRA International, LLC Due...

The Issue: doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake -...

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

Class I — Serious Health HazardOngoing
Refund