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 2928129300 of 55,415 recalls

Medical DeviceDecember 18, 2017· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Cardiovascular Procedure Kits containing Pall LG6NS LeukoGuard¿...

The Issue: Possible blood leaks through the hydrophobic portion of the Pall LG6NS...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical...

The Issue: Complaints have been received concerning questionable results on analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Phadia US Inc

Recalled Item: ImmunoCAP Allergen c5 Recalled by Phadia US Inc Due to The stability...

The Issue: The stability specifications of ImmunoCAP Allergen c5, Ampicilloyl were not met.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Roche Diagnostics Corporation

Recalled Item: c6000 Recalled by Roche Diagnostics Corporation Due to Complaints have been...

The Issue: Complaints have been received concerning questionable results on analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Phadia US Inc

Recalled Item: ImmunoCAP Allergen c6 Recalled by Phadia US Inc Due to The stability...

The Issue: The stability specifications of ImmunoCAP Allergen c6, Amoxicilloyl were not...

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

Class II — Potential Health HazardOngoing
FoodDecember 18, 2017· Meijer Distribution, Inc

Recalled Item: Meijer Michigan Harvest Salad 10 Oz retail unit in plastic Recalled by...

The Issue: Sliced apples within the products being potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2017· Meijer Distribution, Inc

Recalled Item: Meijer Sharable Waldorf Salad 16 Oz retail unit in plastic Recalled by...

The Issue: Sliced apples within the products being potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2017· Gel Spice Co, Inc.

Recalled Item: Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) Recalled by Gel...

The Issue: Gel Spice, Inc. is recalling three beef flavored bouillon cube products...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2017· Gel Spice Co, Inc.

Recalled Item: Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) Recalled by Gel...

The Issue: Gel Spice, Inc. is recalling three beef flavored bouillon cube products...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 18, 2017· Meijer Distribution, Inc

Recalled Item: Meijer Fresh Cranberry Apple Stuffing Starter 18.9 Oz retail unit Recalled...

The Issue: Sliced apples within the products being potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 18, 2017· Osmotica Pharmaceutical Corp

Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugDecember 18, 2017· Osmotica Pharmaceutical Corp

Recalled Item: Methylphenidate Hydrochloride Extended-release Tablets Recalled by Osmotica...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 18, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....

The Issue: Package integrity failure observed during routine shift package integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Model 882482 Product Usage: BrightView XCT is a Recalled by...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· GE Healthcare, LLC

Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...

The Issue: if the cables of the Monica IF24 System are removed by a user, and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Recalled...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· GE Healthcare, LLC

Recalled Item: Uterine Electromyographic Monitor - Monica Novii Wireless Patch System...

The Issue: if the cables of the Monica Novii System are removed by a user, and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Recalled...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing