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 10021–10040 of 29,737 recalls

Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Medex 10 IN Pressure Injector Line w/Rot (1200psi) NS. Recalled by Smiths...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Soft Computer Consultants, Inc.

Recalled Item: SoftCytogenetics Recalled by Soft Computer Consultants, Inc. Due to Software...

The Issue: Software is given wrong results going out to HIS on test that had reruns.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: LogiCal Left Heart Kit Recalled by Smiths Medical ASD Inc. Due to Specific...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: AM12M Acquisition Module accessory. Impacted software version of the AM12M...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Smiths Medical ASD Inc.

Recalled Item: Manifold rotator (Component): a. 250 2 GANG MANIFOLD ROTATOR Recalled by...

The Issue: Specific lots of Medex High Pressure Adaptors, Rotators, Manifolds,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2021· Welch Allyn Inc Mortara

Recalled Item: Surveyor S12/S19 Bedside Patient Monitor Recalled by Welch Allyn Inc Mortara...

The Issue: Devices do not meet IEC 60601-2-27 requirements as labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...

The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for Recalled by...

The Issue: 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Atos Medical AB

Recalled Item: Provox Life Night HME Recalled by Atos Medical AB Due to Provox Life Night...

The Issue: Provox Life Night HME may be incorrectly inserted sideways or forcefully...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Philips North America Llc

Recalled Item: Philips Xper Flex Cardio (FC2010 Recalled by Philips North America Llc Due...

The Issue: Performance issues with the Xper Flex Cardio Physio Monitoring System...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Recalled by Nobel Biocare...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75...

The Issue: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Radiometer Medical ApS

Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...

The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...

The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· ROi CPS LLC

Recalled Item: Regard Dressing Change Tray Recalled by ROi CPS LLC Due to ChloraPrep...

The Issue: ChloraPrep applicators in the kit can grow organisms that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number:...

The Issue: Some Artis zee ceiling systems show an increased abrasion of the cabling at...

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

Class II — Potential Health HazardOngoing