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. 2,731 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,731 in last 12 months

Showing 1216112180 of 30,087 recalls

Medical DeviceApril 24, 2020· Physio-Control, Inc.

Recalled Item: Infant/Child Reduced Energy Defibrillation Electrodes Recalled by...

The Issue: Packaging of infant child reduced energy electrodes was not properly sealed.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· Abbott Gmbh & Co. KG

Recalled Item: ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained...

The Issue: Abbott identified that samples tested for ARCHITECT STAT High Sensitive...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Olympus Corporation of the Americas

Recalled Item: OLYMPUS ShockPulse-SE Lithotripsy System Recalled by Olympus Corporation of...

The Issue: A component of the Olympus ShockPulse Transducer was manufactured with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Philips North America, LLC

Recalled Item: ProxiDiagnost N90 Recalled by Philips North America, LLC Due to The thermo...

The Issue: The thermo switches in the three-phase transformer, which normally aid in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2020· LABORIE MEDICAL TECHNOLOGIES, CANADA ULC

Recalled Item: Pump Tube Set for MMS Libra and Solar Systems - Recalled by LABORIE MEDICAL...

The Issue: This field correction is being initiated to address potentially damaged...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2020· BIOSENSE WEBSTER

Recalled Item: PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only Recalled...

The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2020· BIOSENSE WEBSTER

Recalled Item: PENTARAY NAV eco HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx Recalled...

The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 -...

The Issue: If the C-arm leaves its intended travel path due to a fault within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing