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. 2,794 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,794 in last 12 months

Showing 70217040 of 54,363 recalls

Medical DeviceJanuary 26, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with:...

The Issue: Due to a trend in false positive Candida tropicalis results on blood culture...

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

Class II — Potential Health HazardOngoing
FoodJanuary 25, 2024· Lidl US TRADING

Recalled Item: Banana Pepper Rings 16 FL OZ (1PT) 473ml . Packaged Recalled by Lidl US...

The Issue: Container integrity issued (punctured lid)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
DrugJanuary 25, 2024· Alpha Aromatics

Recalled Item: Pure Care Foaming Mint Hand Sanitizer 62% Recalled by Alpha Aromatics Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 25, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35 Recalled by...

The Issue: Discoloration: discolored tablets (shades of blue) mixed in with the white...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 25, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Nortrel 7/7/7 (norethindrone and ethinyl estradiol tablets USP- triphasic...

The Issue: Discoloration: discolored tablets (shades of blue) mixed in with the white...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 25, 2024· Amerisource Health Services LLC

Recalled Item: Febuxostat Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 25, 2024· Raye's Inc.

Recalled Item: SW Bari Lift & Transfer Recalled by Raye's Inc. Due to Retrospective...

The Issue: Retrospective engineering analysis against current ISO standards for hoists...

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

Class II — Potential Health HazardOngoing
FoodJanuary 24, 2024· Mutti USA Inc.

Recalled Item: MUTTI Crushed Tomatoes Recalled by Mutti USA Inc. Due to Internal can lining...

The Issue: Internal can lining is detaching from can into product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 24, 2024· Thommen Medical AG

Recalled Item: impression coping Recalled by Thommen Medical AG Due to The depth of the...

The Issue: The depth of the internal canal was not manufactured according to...

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: 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