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. 2,806 recalls have been distributed to Ohio in the last 12 months.
Showing 3281–3300 of 30,087 recalls
Recalled Item: Biodesign Fistula Plug C-FPS-0.2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPB-0.4 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essentia MAJ Laparotomy Std Pack Recalled by American Contract Systems, Inc....
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Day Surgery General Pack Recalled by American Contract Systems, Inc. Due to...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.2-2 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.4 - For implantation to reinforce...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.7 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthroscopy Pack Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Open Shoulder Recalled by American Contract Systems, Inc. Due to ACS...
The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft...
The Issue: Products expire prior to the expiration date printed on the product labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FILMARRAY 2.0 INSTRUMENT Recalled by BioFire Diagnostics, LLC Due to...
The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FILMARRAY TORCH MODULE BOX Recalled by BioFire Diagnostics, LLC Due to...
The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety Recalled...
The Issue: The syringes that were inadvertently shipped from the Distribution Center....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion 7M20 systems with FlexArm ceiling-mounted system Recalled by...
The Issue: The motorized longitudinal movement of the FlexArm stand may be inconsistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ERIC Retrieval Device ER174030 ER176044 The ERIC Retrieval Recalled by...
The Issue: Due to Retrieval Device product labels stating the incorrect expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pump 371 14F LT CMR Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pump 381 Pump Set (US) Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 SmartAssist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Pump 371 Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImpellaCP SmartAssistSetAPAC Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.