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 3304133060 of 55,415 recalls

DrugMarch 7, 2017· Legacy Pharmaceutical Packaging LLC

Recalled Item: ATENOLOL Tablets Recalled by Legacy Pharmaceutical Packaging LLC Due to...

The Issue: Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2017· Pfizer Inc

Recalled Item: Quillivant XR (methylphenidate HCl) for extended-release oral suspension...

The Issue: Failed Dissolution Specifications: Dissolution at 8 hour was out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended-Release Tablets Recalled by Alvogen, Inc Due...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Pfizer Inc

Recalled Item: Quillivant XR (methylphenidate HCl) for extended-release oral suspension...

The Issue: Failed Dissolution Specifications: Dissolution at 8 hour was out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended Release Tablets Recalled by Alvogen, Inc Due...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Pfizer Inc

Recalled Item: Quillivant XR (methylphenidate HCl) for extended-release oral suspension...

The Issue: Failed Dissolution Specifications: Dissolution at 8 hour was out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended-Release Tablets Recalled by Alvogen, Inc Due...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended-Release Tablets Recalled by Alvogen, Inc Due...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended Release Tablets 30 mg Recalled by Alvogen,...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended-Release Tablets Recalled by Alvogen, Inc Due...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 7, 2017· Ulrich Medical USA Inc

Recalled Item: uNion Cervical Plate System Product Usage: The uNion Cervical Plate Recalled...

The Issue: Surgical technique was revised to prevent static plate screws blocking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2017· BioMerieux SA

Recalled Item: NucliSENS Lysis Buffer Recalled by BioMerieux SA Due to Problem with colored...

The Issue: Problem with colored eluates for whole blood extractions

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2017· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: Specimen Gate Laboratory Recalled by PerkinElmer Life and Analytical...

The Issue: Potential for errors in patient results generated by the Specimen Gate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352...

The Issue: Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically...

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

Class II — Potential Health HazardOngoing
DrugMarch 6, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: ATENOLOL Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of...

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

Class II — Potential Health HazardOngoing
Refund