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. 2,487 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,487 in last 12 months

Showing 4972149740 of 55,415 recalls

Medical DeviceAugust 22, 2013· ITC-Nexus Dx

Recalled Item: Surgicutt fully automated incision making device for bleeding time...

The Issue: ITC has determined that the blade in their Surgicutt with Blotting Paper...

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

Class II — Potential Health HazardOngoing
DrugAugust 21, 2013· Actavis South Atlantic LLC

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by Actavis...

The Issue: Failed Dissolution Specifications: This recall is an extension of the recall...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 5 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 2 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Breakpoint Combo 7 Product Usage:...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: MicroscanrapID/S panels NC3.11 Sold in Japan only. Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Breakpoint Combo 4 Sold outside of US Recalled by...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Urine Combo 4 Sold outside of US Recalled by Siemens...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Combo 2 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan Synergies Plus Negative Urine Combo 1 Product Usage: MicroScan¿...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan rapID/S panels NC3.12 Sold in Japan only. Product Usage: Recalled...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan plus Negative Combo 3 Sold outside of US only. Recalled by Siemens...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Microscan rapID/S panels NC3.33 Sold in Japan only. Product Usage: Recalled...

The Issue: Confirmed increase in false susceptible and false intermediate misreads for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 20, 2013· Carestream Health Inc.

Recalled Item: Carestream DRX Evolution System (Standard Q) The DRX-Evolution System...

The Issue: Carestream received a report of an exposure being initiated without a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2013· Iba Dosimetry Gmbh

Recalled Item: iba COMPASS SW Version 3.0 Recalled by Iba Dosimetry Gmbh Due to The...

The Issue: The development partner of IBA informed that there is problem in a SW...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHECK FastClix Lancing Device. It is intended for use in Recalled by...

The Issue: Internal Roche inspections have revealed that after the lancet is used for a...

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

Class II — Potential Health HazardOngoing
DrugAugust 17, 2013· Amneal Pharmaceuticals of New York, LLC.

Recalled Item: Extended Phenytoin Sodium Capsules Recalled by Amneal Pharmaceuticals of New...

The Issue: Failed dissolution specifications; 18 month CRT

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 16, 2013· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of assurance of...

The Issue: Lack of assurance of sterility: ineffective crimp on fliptop vials that may...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 16, 2013· Atlantic Pro Nutrients, Inc. dba XYMOGEN

Recalled Item: LipiChol 540 (Omega-3 Phospholipid) Medical Food Dispense by Prescription...

The Issue: Product was labeled as a medical food as opposed to a dietary supplement.

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

Class III — Low RiskOngoing
Refund
FoodAugust 16, 2013· Atlantic Pro Nutrients, Inc. dba XYMOGEN

Recalled Item: XYMOGEN LipiChol (Omega-3 Phospholipid 540 mg) Medical Food Distributed by...

The Issue: Product was labeled as a medical food as opposed to a dietary supplement.

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

Class III — Low RiskOngoing
Refund