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. 1,154 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,154 in last 12 months

Showing 1741–1760 of 54,363 recalls

DrugAugust 4, 2025· PFIZER INC

Recalled Item: Vial Label: Epinephrine Injection Recalled by PFIZER INC Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2025· B BRAUN MEDICAL INC

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...

The Issue: Lack of Assurance of Sterility; potential for fluid leakage at one of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 4, 2025· PFIZER INC

Recalled Item: Vial Label: 8.4% Sodium Bicarbonate Injection Recalled by PFIZER INC Due to...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 4, 2025· Merit Medical Systems, Inc.

Recalled Item: PhD Hemostasis Valve Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Hemostasis valve has a manufacturing defect and when used the valve cap may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series....

The Issue: Potential that a component (air baffle) may be missing in some Nehalem...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
FoodAugust 1, 2025· SRI SRI TATTVA

Recalled Item: Sri Sri Tattva Recalled by SRI SRI TATTVA Due to Undeclared Soy

The Issue: Product contains undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee System Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...

The Issue: Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2025· Lumicell, Inc.

Recalled Item: Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product...

The Issue: The potential of the elastic bands included in the kit detaching or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: B12 Methylcobalamin for Injection Recalled by GenoGenix LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Elite Stack MSC Exosome Reconstitution Solution for Injection Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Elite Stack Reconstitution Solution for Injection Recalled by GenoGenix LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Proline for Injection Recalled by GenoGenix LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: B5 Dexpanthenol for Injection Recalled by GenoGenix LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund