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. 2,592 recalls have been distributed to Ohio in the last 12 months.
Showing 24001–24020 of 55,415 recalls
Recalled Item: AQUACIL instant foaming hand sanitizer Recalled by Inopak Ltd Due to CGMP...
The Issue: CGMP Deviations: hand sanitizers and soaps were not produced under current...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1...
The Issue: Possibility that a suture raw material containing high endotoxin levels was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...
The Issue: Possibility that a suture raw material containing high endotoxin levels was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Isopure Sodium Bicarbonate Mixing and Distribution System (IsoMix PRO) with...
The Issue: There is a potential for an uneven plastic encapsulation of the magnet ring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Recalled by AURIS HEALTH INC Due to Reports of aspirating biopsy...
The Issue: Reports of aspirating biopsy needle breakage
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acidified Concentrate Distribution and Storage System (ACDS System) with a...
The Issue: There is a potential for an uneven plastic encapsulation of the magnet ring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Finish Thompson Centrifugal Pump Model #110192-3 (sold as spare part)...
The Issue: There is a potential for an uneven plastic encapsulation of the magnet ring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace PACS 4.4 Recalled by Philips Healthcare Informatics, Inc. Due...
The Issue: Images may potentially become corrupt while using the system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FENTANYL Transdermal System Recalled by Alvogen, Inc Due to Product Mix-Up:...
The Issue: Product Mix-Up: Customer complaint that their carton labeled as Fentanyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This...
The Issue: Defective Delivery System: difficult to express
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.