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. 1,118 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,118 in last 12 months

Showing 13701–13720 of 30,087 recalls

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· 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· 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 26, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci SP Surgical System Recalled by Intuitive Surgical, Inc. Due to The...

The Issue: The firm become aware of a potentially defective capacitors on circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci X Surgical System Surgical System Recalled by Intuitive Surgical,...

The Issue: The firm become aware of a potentially defective capacitors on circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2019· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Surgical System Recalled by Intuitive Surgical,...

The Issue: The firm become aware of a potentially defective capacitors on circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2019· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed Carestation CS1 - Product Usage: The device can Recalled by...

The Issue: Fasteners potentially torqued to a value less than the specified value and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed...

The Issue: SOMATOM Definition Edge, SOMATOM Definition AS, SOMATOM Definition Flash...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· Stryker GmbH

Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...

The Issue: The seal integrity of the sterile bag containing the kits may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: HS70A Diagnostic Ultrasound System Version 2.01.00 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2019· NeuroLogica Corporation

Recalled Item: WS80A Diagnostic Ultrasound System Version 1.00.16 Recalled by NeuroLogica...

The Issue: There is a potential for probes overheating when decreasing the Doppler SV...

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

Class II — Potential Health HazardOngoing