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. 2,807 recalls have been distributed to Ohio in the last 12 months.
Showing 1261–1280 of 30,087 recalls
Recalled Item: Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Recalled by THOR...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlantis IO FLO Product Name: Atlantis IO FLO-S Recalled by...
The Issue: The defect in the thread area will not allow the device to fully engage with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Recalled by...
The Issue: The defect in the thread area will not allow the device to fully engage with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Recalled by THOR...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software...
The Issue: The potential for a failed welded nut to shear off. When this occurs, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOTAK RELIANCE G/SG with 4-SITE Connector Recalled by Boston Scientific...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELIANCE 4-FRONT Recalled by Boston Scientific Corporation Due to Affected...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOTAK RELIANCE G/SG Recalled by Boston Scientific Corporation Due to...
The Issue: Affected lead models may experience gradually rising LVSI measurements in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK CR2 Part / Catalog Numbers / UDI-DI code: CR2-2-001451 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Model RXM1000 UDI Codes: (01)00860003983812(11)230504(21)X11001...
The Issue: Due to incorrect software configuration that potentially allows more than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 Recalled by...
The Issue: Due to required inspections not being performed on products/units that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bartels ELISA Legionella Urinary Antigen. Model Number: B1029-440. In Vitro...
The Issue: Potential for Bartels ELISA Legionella Urinary Antigen kit B1029-440 lot 065...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CELSITE Product Name: CELSITE BABYPORT SET PUR 4 Recalled by...
The Issue: The potential for minor injury such as damage to the vessel and/or tearing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Operated infusion pumps. t:slim X2 G5 Recalled by Tandem Diabetes...
The Issue: Insulin pumps manufactured with speakers from Revision A and B may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Satellite. Product Code: All . All software versions. The Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.