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 2994129960 of 55,415 recalls

DrugSeptember 27, 2017· United Pharmacy

Recalled Item: Glutamine Recalled by United Pharmacy Due to CGMP Deviations; FDA analysis...

The Issue: CGMP Deviations; FDA analysis deterrmined that the product does not contain...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 27, 2017· WalkMed, LLC

Recalled Item: Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Recalled...

The Issue: There have been reported incidents of fluid leaks at the luer connection....

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

Class II — Potential Health HazardOngoing
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in Recalled by Pharmedium...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: HYDROmorphone HCl in 0.9% Sodium Chloride Injection Recalled by Pharmedium...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· The Harvard Drug Group

Recalled Item: Alprazolam Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2017· Integra LifeSciences Corp.

Recalled Item: Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System...

The Issue: A faulty footswitch may result in unintended ultrasonic fragmentation...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2017· Mobius Imaging, LLC

Recalled Item: AIRO Mobile CT System Recalled by Mobius Imaging, LLC Due to If the...

The Issue: If the tilt-drive motor has an intermittent connection or broken encoder or...

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

Class II — Potential Health HazardOngoing
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Precision Dose Inc.

Recalled Item: Carbamazepine Oral Suspension USP Recalled by Precision Dose Inc. Due to...

The Issue: Subpotent Drug: low out of specification results.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· RXQ Compounding LLC

Recalled Item: methylPREDNIsolone ACETATE Recalled by RXQ Compounding LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility; autoclave parameters were not correct for...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2017· Sandoz Inc

Recalled Item: Ampicillin for Injection Recalled by Sandoz Inc Due to Labeling: Missing...

The Issue: Labeling: Missing Label: customer complaint that some vials of ampicillin...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 25, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Recalled...

The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented...

The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer....

The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...

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

Class II — Potential Health HazardOngoing
DrugSeptember 22, 2017· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Mobic (meloxicam) tablets Recalled by Boehringer Ingelheim Pharmaceuticals,...

The Issue: Labeling: Incorrect or missing package insert. One lot of Mobic Tablets is...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 22, 2017· Silver Spring Foods, Inc.

Recalled Item: waterfront Bistro Tatar Sauce Recalled by Silver Spring Foods, Inc. Due to...

The Issue: Silver Spring is recalling Waterfront Bistro Tartar Sauce because an...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 22, 2017· Guangzhou Improve Medical Instruments Co., Ltd.

Recalled Item: Prevent G Safety Winged Blood Collection Set Glide - Rx Recalled by...

The Issue: Complain due to the hub needle came out when the nurse draw the blood and...

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

Class II — Potential Health HazardOngoing