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. 2,561 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,561 in last 12 months

Showing 3280132820 of 55,415 recalls

DrugMarch 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· Novartis Pharmaceuticals Corp.

Recalled Item: Pilocarpine Hydrochloride Ophthalmic Solution 4% Recalled by Novartis...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2017· GlaxoSmithKline, LLC

Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Aerosol Recalled by...

The Issue: Defective Delivery System: Elevated number of units with out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2017· Novartis Pharmaceuticals Corp.

Recalled Item: Isopto Carpine (pilocarpine hydrochloride opthalmic solution) 4% Recalled by...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 22, 2017· Tosoh Bioscience Inc

Recalled Item: AIA-360 Analyzer is capable of performing two methods of immunoassay:...

The Issue: The firm has become aware of a potential issue with the AIA-360 analyzer...

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

Class II — Potential Health HazardOngoing
DrugMarch 21, 2017· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Institutional, Inc. (d.b.a....

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2017· Roche Diagnostics Corporation

Recalled Item: Sample probes associated with: cobas 6000 Series System Recalled by Roche...

The Issue: Due to a design change in 2015, corrosion on the sample probe electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arterial Catheterization Kit The Arrow¿ Arterial Catheterization device...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow¿ Access Kit with Maximal Barrier Precautions for use with Recalled by...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology A PICC permits venous access Recalled...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit The Arrow¿...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow(R) Access Kit for use with 4 Fr. Peripherally Inserted Recalled by...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath Recalled...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow¿ VPS¿ Access Kit with Maximal Barrier Precautions for use Recalled by...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing