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 1240112420 of 30,087 recalls

Medical DeviceMarch 20, 2020· Physio-Control, Inc.

Recalled Item: LifePAK 500 Automated External Defibrillator Recalled by Physio-Control,...

The Issue: Automated External Defibrillators may not detect a patient connection due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2020· Utak Laboratories Inc

Recalled Item: Utak NR Trace Elements Serum Control Recalled by Utak Laboratories Inc Due...

The Issue: The product has an incorrect value for cadmium and an incorrect expected range.

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

Class III — Low RiskOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: H12+ and patient cable for the H12+ Holter Recorders with Recalled by WELCH...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: S4 and patient cable for the S4 Wireless Telemeter with Recalled by WELCH...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: X12+ and patient cable for the X12+ Telemeter with the Recalled by WELCH...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Lead diagnostic electrocardiograph under the following device names: ELI 10...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor Recalled...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Replaceable lead set for the Wireless Acquisition Module (WAM) Recalled by...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: T12. Incorporates wireless electrocardiographic technology to achieve the...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Q-Tel. The Q-Tel RMS system is a computer-based cardiac and Recalled by...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: ELI PC. The ELI PC Service automatically converts resting ECG Recalled by...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Radiometer Medical ApS

Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...

The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Clip Applier Kit Recalled by Applied Medical Resources Corp Due to There may...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Bard Peripheral Vascular Inc

Recalled Item: Jamshidi Bone Marrow Biopsy/Aspiration Needle Recalled by Bard Peripheral...

The Issue: Sterility compromised due to packaging pouches that may not be sealed properly

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: DR. THAMES - LAP CHOLE Recalled by Applied Medical Resources Corp Due to...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing