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. 1,967 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,967 in last 12 months

Showing 1718117200 of 30,087 recalls

Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: PROXIMALE - 18 cm (7") Appx 0.92 ml Recalled by ICU Medical de Mexico, S.A....

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 191 cm (75") Appx 2.9 ml Recalled by ICU Medical de Mexico, S.A. de C.V. Due...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 20 cm (8") PUR Smallbore Ext Set w/3-Port NanoClave Manifold Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave Manifold Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave Manifold (Orange Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave Manifold Recalled by ICU Medical de...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: DISTALE - 203 cm (80") Bifuse Ext Set w/6 Gang 1o2 Manifold Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 165 cm (65") PUR Smallbore Ext Set w/3-Port NanoClave Manifold Recalled by...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 216 cm (85") PVC/PUR Smallbore Bifuse Ext Set w/3-Port NanoClave Manifold...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 61 cm (24") Smallbore Ext Set w/6-Port NanoClave Manifold Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 43 cm (17") Smallbore Ext Set w/3-Port NanoClave Manifold Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave Manifold (Orange Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 11" Smallbore Ext Set w/NanoClave Recalled by ICU Medical de Mexico, S.A. de...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 28 cm (11") PUR Bifuse Ext Set w/6-Port NanoClave Manifold Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 6" Smallbore Ext Set w/6-Port NanoClave Manifold Recalled by ICU Medical de...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· bioMerieux, Inc.

Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to Several complaints were...

The Issue: Several complaints were received for invalid calibration with low calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius MRI Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Premium Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro M Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing