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. 2,555 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,555 in last 12 months

Showing 3444134460 of 55,415 recalls

Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray Recalled by...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
DrugNovember 7, 2016· Pfizer Inc.

Recalled Item: LEVOXYL(R) (levothyroxine sodium tablets Recalled by Pfizer Inc. Due to...

The Issue: Superpotent

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 7, 2016· Shri Shiva Foods Inc

Recalled Item: MTR MASALA Sambar Powder Recalled by Shri Shiva Foods Inc Due to Potential...

The Issue: The firm distributed a product prior to FDA release for an article which...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 7, 2016· Meijer, Inc.

Recalled Item: Meijer Almonds Salted Caramel Recalled by Meijer, Inc. Due to Undeclared...

The Issue: Meijer initiated a voluntary recall of Meijer Almonds Salted Caramel on...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 7, 2016· Cincinnati Sub-Zero Products Inc

Recalled Item: The Hemotherm 400CE 115v Recalled by Cincinnati Sub-Zero Products Inc Due to...

The Issue: The device may not maintain water flow or temperature control.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Helena Laboratories, Inc.

Recalled Item: Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase...

The Issue: Due to a customer experiencing complaints on bone fraction of assay not...

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

Class III — Low RiskOngoing
Medical DeviceNovember 7, 2016· Tosoh Bioscience, Inc.

Recalled Item: Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing. Recalled by Tosoh...

The Issue: The device defect associated with this recall may result in HbA1c values...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Bayer Healthcare

Recalled Item: MEDRAD Intego PET Infusion System - Pump Intended to deliver Recalled by...

The Issue: Bayer has determined that all current Source Administration Sets (SAS) used...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: Alteon Neck Preserving Stem Recalled by Exactech, Inc. Due to Products were...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: Novation Cemented Plus Femoral Stem Recalled by Exactech, Inc. Due to...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Becton Dickinson & Company

Recalled Item: BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is Recalled by...

The Issue: BD is conducting a voluntary product recall of the BD Spinal Anesthesia...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· DeRoyal Industries Inc

Recalled Item: TENNIS ELBOW SUPPORT Recalled by DeRoyal Industries Inc Due to DeRoyal...

The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· DeRoyal Industries Inc

Recalled Item: PNEUGEL(R) TENNIS ELBOW STRAP Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: Z6Ms transesophageal transducers used on ACUSON SC2000 ultrasound systems...

The Issue: Firm received reports about "acquisition errors" and the deterioration of...

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

Class II — Potential Health HazardOngoing
DrugNovember 4, 2016· West-Ward Pharmaceuticals Corp.

Recalled Item: Amoxicillin for Oral suspension Recalled by West-Ward Pharmaceuticals Corp....

The Issue: Labeling: Label Error on Declared Strength: Some bottles miss a color coded...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 4, 2016· Thayer Intellectual Property, Inc.

Recalled Item: MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a Recalled...

The Issue: The firm failed to notify current customers of IFU update/warning. During a...

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

Class II — Potential Health HazardOngoing
DrugNovember 3, 2016· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: OOS results for known compound.

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 3, 2016· Voco GmbH

Recalled Item: VOCO Futurabond M+ adhesive Recalled by Voco GmbH Due to Labeling mix-up:...

The Issue: Labeling mix-up: Futurabond M+ DCA (Dual Cure Activator) was marked labeled...

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

Class II — Potential Health HazardOngoing