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. 1,042 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,042 in last 12 months

Showing 20101–20120 of 54,363 recalls

Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY Y CONN 3/8 X 3/8 X Recalled by LivaNova...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 1/4X3/16X3/16YCONN Recalled by LivaNova USA Inc. Due to The firm has...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY ASY STR CONN 3/8 STRLE 24 Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY STR CONN 3/16 STRLE 24. REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY 1/4 X 3/8 REDUCER W/LL 24. Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY 1/2 CONN W/LL STRLE 24 REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY CONN Y 1/2X1/2X3/8 STR 24. REF/ Recalled...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· Physio-Control, Inc.

Recalled Item: Infant/Child Reduced Energy Defibrillation Electrodes Recalled by...

The Issue: Packaging of infant child reduced energy electrodes was not properly sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Bone Void Filler Recalled by Medtronic Sofamor Danek USA Inc Due...

The Issue: Product may not maintain its setting characteristics for the labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: Extremities Recalled by Medtronic Sofamor Danek USA Inc Due to Product may...

The Issue: Product may not maintain its setting characteristics for the labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic Bone Void Filler Recalled by Medtronic Sofamor Danek USA Inc Due...

The Issue: Product may not maintain its setting characteristics for the labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Vein Irrigation Cannula with blunt tip. ASY BIC Recalled by LivaNova USA...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY S CONN 3/16X1/8 RDR ANLD24 REF/ Recalled...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 1/4X3/8 REDUC CONN Recalled by LivaNova USA Inc. Due to The firm has...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY RDC Y 1/2X3/8X3/8 STR 24 REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
DrugApril 24, 2020· Dr. Reddy's Laboratories, Inc.

Recalled Item: Esomeprazole Magnesium Delayed Release Capsules USP Recalled by Dr. Reddy's...

The Issue: Discoloration: product contains brown pellets

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2020· QuVa Pharma, Inc.

Recalled Item: R.E.C.K. (Ropivacaine Recalled by QuVa Pharma, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Fresenius Kabi recalling vials of Ketorolac

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2020· Access Scientific LLC

Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...

The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.

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

Class II — Potential Health HazardOngoing