Product Recalls in North Carolina

Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,932 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,932 in last 12 months

Showing 1698117000 of 29,737 recalls

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: 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· 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
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· 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: Kit w/3 Ext Sets Recalled by ICU Medical de Mexico, S.A. de C.V. Due to 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: 38 cm (15") 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: 40 cm (16") 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: 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: 30 cm (12") PUR Bifuse 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: PROXIMALE - 28 cm (11") Smallbore Ext Set w/6-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 DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes may...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Neonatal PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Biomet, Inc.

Recalled Item: Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic...

The Issue: During assembly, an SRS Humeral Distal Body implant failed to engage...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Kit Recalled by Vygon U.S.A. Due to Potential friction holes may affect...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Insertion Tray Recalled by Vygon U.S.A. Due to Potential...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing