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. 2,812 recalls have been distributed to Ohio in the last 12 months.
Showing 21–40 of 55,415 recalls
Recalled Item: Cetrorelix Acetate for Injection (Kit) Recalled by Meitheal Pharmaceuticals,...
The Issue: Defective Delivery System: Missing or duplicated needles within the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...
The Issue: The system labeling (user manual and online labeling) did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artelon FlexBand Dynamic Matrix Recalled by International Life Sciences Due...
The Issue: Augmentation devices failed bacterial endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...
The Issue: The system labeling (user manual and online labeling) did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artelon FlexBand Plus & 41057 Recalled by International Life Sciences Due to...
The Issue: Augmentation devices failed bacterial endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...
The Issue: The system labeling (user manual and online labeling) did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artelon FLEXBAND TWIST .12 3.85x17mm HEX Anchor (Qty Recalled by...
The Issue: Augmentation devices failed bacterial endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...
The Issue: The system labeling (user manual and online labeling) did not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: vancomycin HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ketamine HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: thiamine HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Campy CVA Medium 100/PK Recalled by Remel, Inc Due to Customer complaints...
The Issue: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: acyclovir sodium Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: vancomycin HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: STA Liatest Free Protein S Product Name: STA Recalled by...
The Issue: The potential of out-of-range results and an underestimation of the free...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle...
The Issue: Impactor handle may be missing cross-pin
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep...
The Issue: Label declares bovine colostrum but does not declare milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prime Food Processing Dried Croaker Fish Recalled by Prime Food Processing...
The Issue: Uneviscerated Fish
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit...
The Issue: Impactor handle may be missing cross-pin
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...
The Issue: It was identified that eh Universal Beam Triggering Interface (UBTI) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.