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. 2,779 recalls have been distributed to Ohio in the last 12 months.
Showing 5721–5740 of 55,415 recalls
Recalled Item: Recalled by Stryker Sustainability Solutions Due to Mislabeling
The Issue: Mislabeling; tourniquet cuff packaging labeled as dual port single bladder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP with SmartAssist Recalled by Abiomed, Inc. Due to Nine (9)...
The Issue: Nine (9) Impella CP pumps failed inspection and were inadvertently released.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for...
The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Powerheart G5 AED Recalled by Zoll Medical Corporation Due to G5...
The Issue: G5 Semi-Automatic AED is shipped, with a protective film over its front...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed...
The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Vertix MD - The Vertix MD Trauma has been Recalled by Siemens Medical...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MP - Inended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MP - Intended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Vertix Solitaire - The Vertix MD Trauma has been Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is Recalled by Siemens...
The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size) Recalled by...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Volara System. Single Patient Use (SPU) Circuit 5kit for Volara Recalled by...
The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.