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. 2,808 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,808 in last 12 months

Showing 47814800 of 29,737 recalls

Medical DeviceJanuary 24, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: Opal Recalled by Synthes (USA) Products LLC Due to Products not sterilized,...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: RAPIDSORB IPS Battery Pack Recalled by Synthes (USA) Products LLC Due to...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: 13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX Recalled by Synthes...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: TFNA Femoral Nail 9mm Recalled by Synthes (USA) Products LLC Due to Products...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: 1.5MM Drill Bit/QC/85MM Sterile-surgical Recalled by Synthes (USA) Products...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: VA-LCP Clavicle Plate 2.7 Recalled by Synthes (USA) Products LLC Due to...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: 2.5MM DRILL BIT/QC/GOLD/110MM STERILE-surgical Recalled by Synthes (USA)...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: RIA Tube Assembly Recalled by Synthes (USA) Products LLC Due to Products not...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2024· Synthes (USA) Products LLC

Recalled Item: TFNA Femoral Nail 11mm Recalled by Synthes (USA) Products LLC Due to...

The Issue: Products not sterilized, sterility cannot be confirmed

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: stay-safe /Luer Lock Adapter 4 in Recalled by Fresenius Medical Care...

The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 23, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: stay-safe /Luer Lock Catheter Ext. 18 in Recalled by Fresenius Medical Care...

The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 23, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: stay-safe /Luer Catheter Ext. 6 in Recalled by Fresenius Medical Care...

The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 23, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: stay-safe /Luer Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...

The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 23, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: stay-safe /Safe Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...

The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 23, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CVS Health Waterproof Wound Tracking Dressing Recalled by MEDLINE...

The Issue: Product failed sterility testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2024· SEDECAL SA

Recalled Item: Battery Mobile X-ray Unit EASY MOVING Model with telescopic column 3.1...

The Issue: Potential interference with the anti-fall system.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2024· Invacare Corporation

Recalled Item: Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component...

The Issue: Invacare Homecare & G-Series Bed Components identified with a potential weld...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS 5600 Integrated System (New and ) Recalled by Ortho-Clinical...

The Issue: Potential For Aspiration from Unintended Sample Container During Sampling...

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

Class II — Potential Health HazardOngoing