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. 1,146 recalls have been distributed to Ohio in the last 12 months.
Showing 6981–7000 of 30,087 recalls
Recalled Item: ACL ELITE PRO-Analyzer designed specifically for clinical use in the...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL ELITE designed specifically for clinical use in the Recalled by...
The Issue: Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATITUDE NXT Remote Patient Management System Recalled by Boston Scientific...
The Issue: Under specific circumstances, the U.S. product registration system did not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno systems with a Siemens Healthineers table or Trumpf/MAQUET...
The Issue: If, during the procedure, X-ray has been released and a image has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EndoHPB Bipolar Radiofrequency (RF) Catheter 8F (2.7mm). A...
The Issue: Cease use of the Habib EndoHPB Bipolar RF Catheter with the ERBE VIO3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno systems with a Siemens Healthineers table or a Recalled by...
The Issue: In the event of any unintended table movement, the system may not detect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOLOC 3DSi CLAW II 4 HOLE Plate Recalled by Wright Medical Technology,...
The Issue: Stryker has identified an issue that impacts two specific lots of CLAW" II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOLOC 3DSi CLAW II 4 HOLE Plate Recalled by Wright Medical Technology,...
The Issue: Stryker has identified an issue that impacts two specific lots of CLAW" II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEAR Implant (Bridge-Enhanced ACL Restoration) Recalled by Miach...
The Issue: The field action was initiated in February of 2023 and was limited to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 0.5mL Recalled by Becton Dickinson & Company...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution Recalled by...
The Issue: MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPHEN Protein C 5 kit is for in vitro quantitative Recalled by Aniara...
The Issue: New warnings and precautionary statements on product labelling: Reagent 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREAT NOBIL GRIP Recalled by Preat Corp Due to Product is labeled with an...
The Issue: Product is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Recalled...
The Issue: TFNA Femoral Nails labeled and etched as 200mm may measure 170mm in length,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - Recalled by BioFire...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml Recalled by...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1)...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - Recalled by BioFire...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.