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. 1,064 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,064 in last 12 months

Showing 17481–17500 of 54,363 recalls

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 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 Dual Aspirate (SMN 11314045) - 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 DAA AUTOSAMPLER (SMN 10374454) - 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 2120i Dual Aspirate Autosampler (SMN 10285573) - 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 (RoHS) with Single Aspirate Autosampler (SMN 11219529) - OUS...

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 Dual Aspirate Autosampler (SMN 10285573) - 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 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) - 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 2120 SAA AUTOSAMPLER (SMN 10374453) - 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 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
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· Covidien

Recalled Item: Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical...

The Issue: Investigations related to customer complaints received for particulate...

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 4, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Sensis/ Sensis Vibe Hemo systems with VD12A software as follows: Recalled by...

The Issue: Due to the configuration of certain Windows Service Permissions within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2021· Covidien, LP

Recalled Item: Covidien Signia Small Diameter Curved Tip Intelligent Reload 45 mm Recalled...

The Issue: Potential for the device safety interlock to fail. The safety interlock...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2021· Covidien, LP

Recalled Item: Covidien Signia Small Diameter Curved Tip Intelligent Reload 30 mm Recalled...

The Issue: Potential for the device safety interlock to fail. The safety interlock...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2021· Covidien, LP

Recalled Item: Covidien Signia Grey Small Diameter Curved Tip Intelligent Reload 30...

The Issue: Potential for the device safety interlock to fail. The safety interlock...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2021· ROi CPS LLC

Recalled Item: Regard Recalled by ROi CPS LLC Due to ROi CPS, LLC has become aware, through...

The Issue: ROi CPS, LLC has become aware, through a vendor issued urgent medical device...

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

Class II — Potential Health HazardOngoing
DrugMarch 4, 2021· Teva Pharmaceuticals USA

Recalled Item: Romidepsin Injecton Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurity/Degradation Specifications: Out-of-specifications results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund