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. 1,866 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,866 in last 12 months

Showing 3606136080 of 55,415 recalls

Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# e4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· LeMaitre Vascular, Inc.

Recalled Item: AnastoCiip Universal Clip Remover (1Each} REF# 4001-04 The Anastoclip Clip...

The Issue: US marketing brochure for the AnastoClip AC Closure System states that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Nobel Biocare Usa Llc

Recalled Item: Replace Select Tapered TiU NP 3.5x11.5mm Recalled by Nobel Biocare Usa Llc...

The Issue: Incorrect top label on an implant package.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2016· Sorin Group USA, Inc.

Recalled Item: AORTIC ARCH CANNULA Recalled by Sorin Group USA, Inc. Due to Sorin Group USA...

The Issue: Sorin Group USA is recalling Aortic Arch Cannulae (part numbers NA-55X7 and...

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

Class II — Potential Health HazardOngoing
FoodJune 21, 2016· Kill Cliff

Recalled Item: KC (Kill Cliff) Strawberries & Cream Protein Bars Recalled by Kill Cliff Due...

The Issue: Product may contain mold. Recall started on 6/21/16

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Dynasty Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Cobalt Chromium Heads Transcend: 26000017 Recalled by MicroPort Orthopedics...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Procotyl (Rim- Lock) Liners: Recalled by MicroPort Orthopedics Inc. Due to...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Shells: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Shell: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Lineage Liners: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· Omega Medical Imaging, Inc.

Recalled Item: 2 over 2 Elevating Monitor Suspension - Omega Medical Imaging Recalled by...

The Issue: Elevating Monitor Suspension separated from the lifting column bracket

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2016· Invacare Corporation

Recalled Item: Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed...

The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2016· Invacare Corporation

Recalled Item: lnvacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16. Packed one...

The Issue: The rear gradation scale was screen printed upside down on the flowmeter gauge.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2016· Medtronic Navigation

Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...

The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...

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

Class II — Potential Health HazardOngoing
DrugJune 17, 2016· Teva North America

Recalled Item: ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL)...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Linezolid Injection 600 mg/300 mL Rx Only Recalled by Teva North America Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Ondansetron Injection USP 40 mg/20 mL (2 mg/mL) Recalled by Teva North...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund