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. 2,542 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,542 in last 12 months

Showing 3606136080 of 55,415 recalls

FoodJune 22, 2016· Wm Bolthouse Farms Inc

Recalled Item: Bolthouse Farms Vanilla Bean Protein Plus: 30 g protein per Recalled by Wm...

The Issue: Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 22, 2016· Wm Bolthouse Farms Inc

Recalled Item: Bolthouse Farms Banana Honey Almond Butter Protein Plus: 30 g Recalled by Wm...

The Issue: Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 22, 2016· Wm Bolthouse Farms Inc

Recalled Item: Bolthouse Farms Coffee Protein Plus: 30 g protein per bottle Recalled by Wm...

The Issue: Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 22, 2016· Wm Bolthouse Farms Inc

Recalled Item: Bolthouse Farms Strawberry Protein Plus: 30 g protein per bottle Recalled by...

The Issue: Bolthouse Farms is recalling 8 varieties of Protein Plus and Perfectly...

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

Class II — Potential Health HazardOngoing
Refund
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: 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· 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: 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 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· 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: 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 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
Medical DeviceJune 17, 2016· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...

The Issue: It is possible that that the selected Plan-of-the Day could be accidently...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA¿ Chemistry (Syva Onboard) Theophylline_2 (THEO_2) Reagent is for in...

The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2016· Integra LifeSciences Corp.

Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...

The Issue: Data from internal studies suggests there may be a potential that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...

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

Class II — Potential Health HazardOngoing