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. 1,887 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,887 in last 12 months

Showing 2824128260 of 29,737 recalls

Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364N...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak Catalog Number: 1364 Chek-Stix¿ Positive and...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 18 Fr 6mm Sft Flow Angled Wire The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Soft Flow Ang W/L The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS) Catalog Number: 1364E...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Str Wire W/L The Sarns Recalled by Terumo Cardiovascular...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens CLINITEK Atlas Positive and Negative Control Strips for Urine...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Straight The Sarns Aortic Cannula Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 18 Fr 6mm Sft Flow Ang Wire W/L The Sarns Recalled by Terumo Cardiovascular...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Straight Wir The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364M...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...

The Issue: Boxes labeled as CIP5 may contain cartridges of AMP5.

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

Class III — Low RiskOngoing
Medical DeviceNovember 20, 2012· GE Healthcare It

Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...

The Issue: GE Healthcare is aware of a potential safety issue associated with the use...

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

Class III — Low RiskOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-222 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. SW-121 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-221 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· ConMed Corporation

Recalled Item: WANG Transbronchial Aspiration Needles Cat. No. MW-322 Recalled by ConMed...

The Issue: ConMed received complaints from a user facility reporting that the WANG...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Intersept Custom Tubing Pack with or without coating ( Recalled by...

The Issue: Medtronic is initiating an Urgent Medical Device Customer Notification. We...

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

Class II — Potential Health HazardOngoing