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. 1,997 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,997 in last 12 months

Showing 1358113600 of 54,363 recalls

DrugApril 21, 2022· McKesson Corporation dba McKesson Drug Company

Recalled Item: Erythromycin Topical Gel USP Recalled by McKesson Corporation dba McKesson...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2022· McKesson Corporation dba McKesson Drug Company

Recalled Item: Halobetasol Propionate Ointment 0.05% Net Wt. Recalled by McKesson...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2022· McKesson Corporation dba McKesson Drug Company

Recalled Item: Lidocaine Prilocaine Cream USP Recalled by McKesson Corporation dba McKesson...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2022· McKesson Corporation dba McKesson Drug Company

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by McKesson Corporation dba...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 21, 2022· Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.)

Recalled Item: ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version...

The Issue: Due to interference with the Live Listen feature of hearing aid or AirPods,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2022· Oakworks Inc

Recalled Item: PX200 Emergency Relief Bed Recalled by Oakworks Inc Due to Product label was...

The Issue: Product label was printed without the UDI number and warning label was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2022· Oakworks Inc

Recalled Item: Oakworks Bed (Emergency Field Bed) Recalled by Oakworks Inc Due to The...

The Issue: The warning label was printed with the incorrect weight capacity. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2022· Baxter Healthcare Corporation

Recalled Item: 15 Liters Drain Bag Recalled by Baxter Healthcare Corporation Due to Certain...

The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2022· Baxter Healthcare Corporation

Recalled Item: 3 Recalled by Baxter Healthcare Corporation Due to Certain Peritoneal...

The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2022· Baxter Healthcare Corporation

Recalled Item: APD Drain Manifold Recalled by Baxter Healthcare Corporation Due to Certain...

The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2022· Baxter Healthcare Corporation

Recalled Item: Locking Cap for PD Catheter Adapter Recalled by Baxter Healthcare...

The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2022· Baxter Healthcare Corporation

Recalled Item: 5 Prong Manifold Set (with Luer Connectors) Recalled by Baxter Healthcare...

The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2022· Baxter Healthcare Corporation

Recalled Item: Effluent Sample Bag Recalled by Baxter Healthcare Corporation Due to Certain...

The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...

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

Class II — Potential Health HazardOngoing
FoodApril 20, 2022· Wegmans Food Markets, Inc.

Recalled Item: Wegmans Food You Feel Good About Lobster Bisque - 16 Recalled by Wegmans...

The Issue: Seafood HACCP plan was not fully implemented.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 20, 2022· Ion Beam Applications S.A.

Recalled Item: Proteus235- Proton Therapy System: to produce and deliver a proton Recalled...

The Issue: First layer of Uniform Scanning treatment fields is sometimes irradiated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2022· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: The C304-HIS device features a guide wire to access the vein Recalled by...

The Issue: The firm's internal processes identified that certain lots may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2022· Medtronic Perfusion Systems

Recalled Item: Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System Recalled by...

The Issue: Firm detected an increase in complaints related to fractured jaw tips of the...

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

Class II — Potential Health HazardOngoing
FoodApril 19, 2022· Doux South Specialties LLC

Recalled Item: DOUX SOUTH PICKLES EAT WITH A SOUTHERN ACCENT BAKKAVOR CURRY Recalled by...

The Issue: The firm received a positive test result for Listeria monocytogenes for the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 19, 2022· Haemonetics Corporation

Recalled Item: Product Name: TEG5000 Analyzer (07-022 Recalled by Haemonetics Corporation...

The Issue: When the TEG 5000 Analyzer including TEG Analytical Software is used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2022· Smith & Nephew Inc

Recalled Item: LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5 Recalled...

The Issue: It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box...

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

Class II — Potential Health HazardOngoing