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. 2,592 recalls have been distributed to Ohio in the last 12 months.
Showing 24461–24480 of 55,415 recalls
Recalled Item: Remifentanil HCl active pharmaceutical ingredient (API) for manufacturing...
The Issue: Failed Impurities/Degradation Specifications: Unknown impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bacitracin 3000U/30 mL Irrigation Recalled by Anderson Compounding Pharmacy,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate 5 mg/3mL Inhalation Recalled by Anderson Compounding...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 11 Recalled by Anderson Compounding Pharmacy, Inc. DBA Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 23 Day Injection Extra Strength Recalled by Anderson Compounding...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin 40 mcg/mL Recalled by Anderson Compounding Pharmacy, Inc. DBA...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin Tri-Mix 2.5:7.5:0.25 Injection Recalled by Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Serum Tears 20% Drops Recalled by Anderson Compounding Pharmacy, Inc. DBA...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: da Vinci SP surgical system Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive has become aware that the da Vinci SP system may trigger a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Incorrect part description contained on an additional label placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...
The Issue: Pin hole package failures compromising sterility of product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...
The Issue: There is a potential for the single use suction valve to come apart and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra...
The Issue: Stability did not meet acceptance criteria for visual appearance during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breads from Anna Yeast Free Bread Mix 18.1oz Recalled by Wholesome Treats,...
The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Breads from Anna Dairy & Corn Free Bread Mix 19oz Recalled by Wholesome...
The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.