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. 2,727 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,727 in last 12 months

Showing 1368113700 of 30,087 recalls

Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan Preformed: a) 3.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan Uncuffed: a) 2.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Hudson RCI Sheridan LTS: a) 4.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Sheridan/HVT Novaplus: a) 7.0 mm Recalled by Teleflex Medical Due to...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Teleflex Medical

Recalled Item: Sheridan/CF Novaplus 7.0 mm Recalled by Teleflex Medical Due to Reported...

The Issue: Reported complaints indicate an increased incidence of specific lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System...

The Issue: Artis zee/Q systems patient tables may potentially have cracks in the table...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· MOTEK MEDICAL B.V.

Recalled Item: Body Weight Support (BWS) Light Recalled by MOTEK MEDICAL B.V. Due to The...

The Issue: The firm discovered a potential manufacturing deviation of the yoke of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· The Binding Site Group, Ltd.

Recalled Item: OPTILITE IgM Kit Recalled by The Binding Site Group, Ltd. Due to There is a...

The Issue: There is a potential that users may experience difficulty validating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2019· ICU Medical Inc

Recalled Item: Infusion Pump I.V. Administration Recalled by ICU Medical Inc Due to...

The Issue: Potential for fluid leakage out of air vents on inline filters on Plum and...

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

Class II — Potential Health HazardOngoing