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. 1,908 recalls have been distributed to Ohio in the last 12 months.
Showing 28061–28080 of 55,415 recalls
Recalled Item: PROLENE SUTURE 30"(75CM) 6-0 BLUE Recalled by Ethicon, Inc. Due to The...
The Issue: The needle associated with certain suture product codes has the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE SUTURE BLUE 4X90CM M1.5 USP 4/0 DA RB-1 +P Recalled by Ethicon, Inc....
The Issue: The needle associated with certain suture product codes has the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE SUTURE 4-36" (90CM) 3-0 BLUE Recalled by Ethicon, Inc. Due to The...
The Issue: The needle associated with certain suture product codes has the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Sodium Slides Recalled by Ortho-Clinical Diagnostics Due to Potential...
The Issue: Potential for positively biased results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan Pos Combo Panel Type 43 Recalled by Beckman Coulter Inc. Due to...
The Issue: The drug dilution sequence for Moxifloxacin printed on the panel is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drainer(R) Centesis Catheters: (a) Recalled by Vascular Solutions, Inc. Due...
The Issue: The supplier of Drainer(R) centesis catheters notified Vascular Solutions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel SUPERPACK CS/ 500 SEG/FLASK Recalled by Thermo Fisher Due to Product...
The Issue: Product may fail performance testing for S aureus ATCC 43300.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) 0.1 mg/day Recalled by Noven...
The Issue: Defective Delivery System: no longer meets the specification for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) 0.0375 mg/day Recalled by Noven...
The Issue: Defective Delivery System: no longer meets the specification for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Synthes Torque Limiting Handle Recalled by Synthes (USA) Products LLC Due to...
The Issue: The adapter may demonstrate a degradation of function as the final products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics North...
The Issue: The MRx monitor/defibrillators could fail to charge because the therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...
The Issue: Ingress of fluids into the device can affect various electronic circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Clip Gun Magazines are packaged in individually sealed pouches...
The Issue: The packaging sterile barrier does not comply with the applicable packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elite HV Introducer Recalled by Galt Medical Corporation Due to The products...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: Cross-contamination of samples has been reported when running the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Drainer Centesis Catheter Recalled by Galt Medical Corporation Due to The...
The Issue: The products listed might contain unsafe levels of bacterial endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.