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 3356133580 of 55,415 recalls

FoodFebruary 4, 2017· MDS Foods Inc

Recalled Item: Provolone Cheese packaged as: (a) Santino Deli Made EZ Provolone Recalled by...

The Issue: Potential cross contamination from a of product collected by the State...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 750 mg added to 250 mL 0.9% Sodium Chloride For IV Use Only...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 750 mg added to 5% Dextrose 250 mL For IV Use Only Recalled...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use Only...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.5 gram added to 5% Dextrose 500 mL Recalled by SCA...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.25 g added to 5% Dextrose 250 mL Bag For IV Use Only...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.5 g added to 0.9% Sodium Chloride 250 Recalled by SCA...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· SCA Pharmaceuticals

Recalled Item: Vancomycin HCl 1.25 g added to 0.9% Sodium Chloride 250 mL Bag For IV Use...

The Issue: Presence of particulate matter - this recall is due to a recent Hospira...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 3, 2017· Apotex Inc.

Recalled Item: CycloSPORINE Capsules Recalled by Apotex Inc. Due to Failed...

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

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 3, 2017· Amerisource Health Services

Recalled Item: GlipiZIDE Extended-release tablets Recalled by Amerisource Health Services...

The Issue: Failed dissolution specifications: Glipizide 2.5 mg ER Tablets exceeded...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 3, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee Recalled by Siemens Medical Solutions USA, Inc Due to Failures can...

The Issue: Failures can result due to a component defect on Artis zee systems with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2017· Heartware

Recalled Item: HeartWare HVAD System Controller The HeartWare Ventricular Assist System...

The Issue: Product recall of all HVAD Controllers currently on the market and to...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The single use devices are provided sterile and do not have an expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2017· Elcam Medical, Inc.

Recalled Item: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w...

The Issue: The stopcock was found to have punctures.

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2017· Sandoz Inc

Recalled Item: Transderm Scop (scopolamine) Transdermal System Recalled by Sandoz Inc Due...

The Issue: Labeling: Incorrect Instructions:outer carton contains the incorrect...

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

Class II — Potential Health HazardOngoing
Refund