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 1278112800 of 30,087 recalls

Medical DeviceJanuary 7, 2020· Care Essentials Pty., Ltd.

Recalled Item: Cocoon Convective Warming System Recalled by Care Essentials Pty., Ltd. Due...

The Issue: Potential for thermal damage near the power cord connector and Power Entry...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Humidity Pack (Qty 5) Recalled by Siemens Healthcare...

The Issue: A software error is causing the analyzer to incorrectly eject affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Humidity Pack (Qty 1) Recalled by Siemens Healthcare...

The Issue: A software error is causing the analyzer to incorrectly eject affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· MEDTECH SAS

Recalled Item: ROSA Brain 3.0 Application-Brain Recalled by MEDTECH SAS Due to Some...

The Issue: Some cross-sectional images from the image acquisitions of the patients head...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2020· MEDTECH SAS

Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...

The Issue: Some cross-sectional images from the image acquisitions of the patients head...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...

The Issue: Lot numbers and products inadvertently not included in the scope of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Zimmer Surgical Inc

Recalled Item: Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC...

The Issue: When inflating/deflating a single bladder, both bladders could potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· DePuy Orthopaedics, Inc.

Recalled Item: SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The Recalled by...

The Issue: The device will not connect to the Specialist 2 Locating Outrigger which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2020· Ethicon, Inc.

Recalled Item: Coated VICRYL (Polyglactin 910) Suture Recalled by Ethicon, Inc. Due to Some...

The Issue: Some sutures in the lot may exhibit a small section of braid fraying, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· ICU Medical, Inc.

Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...

The Issue: Inability for the guidewire to pass through the needles included with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2020· Clinical Diagnostic Solutions, Inc.

Recalled Item: Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075...

The Issue: A mix-up of autosampler tube positions with a possibility of...

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

Class II — Potential Health HazardOngoing