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. 1,955 recalls have been distributed to Ohio in the last 12 months.
Showing 21961–21980 of 30,087 recalls
Recalled Item: Covidien Dover P400 PREM U/M 18FR SIL FLY Item Code: Recalled by Covidien...
The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endobon-Xenograft Granules Recalled by Biomet France SARL Due to...
The Issue: Cytotoxicity tests were not passed at 36 months. Use of Endobon-Xenograft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Howmedica Osteonics Corp. Due to During a review...
The Issue: During a review of the packaging, it was determined that the seal integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EkoSonic Endovascular System Recalled by EKOS Corporation Due to The...
The Issue: The EkoSonic kit, including the individually labeled MicroSonic Device (MSD)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.