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. 1,117 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,117 in last 12 months

Showing 10241–10260 of 29,737 recalls

Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INTICA NEO 7 HF-T DF-1 IS-1 ProMRI Recalled by BIOTRONIK Inc Due...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK IPERIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Iperia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i with Single Aspirate Autosampler (SMN 10488923) - US Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i Single Aspirate (SMN 11314044) - US Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 with Single Aspirate Autosampler (SMN 10316162) - US Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i Single Aspirate (SMN 11314044) - OUS Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 with Single Aspirate Autosampler (SMN 10316162) - OUS Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 Dual Aspirate Autosampler (SMN 10313419) - US Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i (RoHS) with Single Aspirate Autosampler (SMN 11219529) - US...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Howmedica Osteonics Corp.

Recalled Item: Trial Cutting Guide for Triathlon Total Knee System Recalled by Howmedica...

The Issue: The posterior condyle of the Specialty Triathlon TS Trial Cutting Guide(s),...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 SAA AUTOSAMPLER (SMN 10374453) - US Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i (RoHS) Dual Aspirate Autosampler (SMN 11219530) - US Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing