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. 2,756 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,756 in last 12 months

Showing 1154111560 of 29,737 recalls

Medical DeviceJuly 20, 2020· NOBEL BIOCARE SERVICES AG

Recalled Item: NobelReplace Conical Connection (CC) PMC RP 4.3x10mm Recalled by NOBEL...

The Issue: Dental implant cap label may incorrectly indicate implant measurements...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2020· Becton Dickinson & Co.

Recalled Item: BD MAX SARS-CoV-2 Reagents Recalled by Becton Dickinson & Co. Due to BD is...

The Issue: BD is experiencing elevated rates of potential false positive results from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Medtronic Neuromodulation

Recalled Item: Restore Clinician Programmer Application Software Recalled by Medtronic...

The Issue: The original version of the A71100 Restore Clinician Programmer Application...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Diasorin Inc.

Recalled Item: Parvovirus B19 IgG EIA kit Part No. V519IGUS Recalled by Diasorin Inc. Due...

The Issue: Printed label inside the box lid of the Parvovirus has the incorrect Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Materialise N.V.

Recalled Item: Match Point System The Match Point System is intended to Recalled by...

The Issue: The procedure side indicated in the top header of the Shoulder Case Planning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Cytocell Ltd.

Recalled Item: Cytocell LPH533-A NUP98 Distal Probe Green - Product Usage:The NUP98...

The Issue: A low risk of a false positive result being issued with a laboratory...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS Anti-SARS-CoV-2 IgG Reagent Pack Recalled by Ortho Clinical...

The Issue: The reagent bottles may be swapped within the reagent pack, which may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS Anti-SARS-CoV-2 Total Reagent Recalled by Ortho Clinical Diagnostics...

The Issue: The reagent bottles may be swapped within the reagent pack, which may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2020· Oxford Immunotec

Recalled Item: Model No:T-SPOT.TB8 Recalled by Oxford Immunotec Due to Incorrect expiration...

The Issue: Incorrect expiration date included in test kit labeling and/or in Substrate...

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

Class III — Low RiskOngoing
Medical DeviceJuly 16, 2020· Oxford Immunotec

Recalled Item: Model No:T-SPOT.TB50 Recalled by Oxford Immunotec Due to Incorrect...

The Issue: Incorrect expiration date included in test kit labeling and/or in Substrate...

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

Class III — Low RiskOngoing
Medical DeviceJuly 16, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: uEXPLORER PET/CT Diagnostic Imaging System - Product Usage: This system...

The Issue: 1) 1) Potential intermittent issue may cause image data problems, may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: uMI 550 PET/CT Diagnostic Imaging System - Product Usage: This Recalled by...

The Issue: 1) Service function problem may cause false marking of a bad channel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2020· Smith & Nephew, Inc.

Recalled Item: Tibial knee prosthesis Recalled by Smith & Nephew, Inc. Due to Due to an...

The Issue: Due to an inconsistency in the raw material process, specific lots may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· OraSure Technologies, Inc.

Recalled Item: Pointts sistema de ellmlnact! Recalled by OraSure Technologies, Inc. Due to...

The Issue: Unit boxes not properly sealed

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

Class III — Low RiskOngoing
Medical DeviceJuly 15, 2020· OraSure Technologies, Inc.

Recalled Item: Personelle OTC Skin Tag Remover Recalled by OraSure Technologies, Inc. Due...

The Issue: Unit boxes not properly sealed

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

Class III — Low RiskOngoing
Medical DeviceJuly 15, 2020· OraSure Technologies, Inc.

Recalled Item: CVS Advanced Wart Remover Kit Recalled by OraSure Technologies, Inc. Due to...

The Issue: Unit boxes not properly sealed

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

Class III — Low RiskOngoing
Medical DeviceJuly 15, 2020· Hager & Meisinger Gmbh

Recalled Item: SINGLES Carbide US-No. FG556 Recalled by Hager & Meisinger Gmbh Due to...

The Issue: US-dates between the product package label and the bar code display.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· Qiagen Sciences LLC

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA Recalled by Qiagen...

The Issue: There is an increased rate of potential false positive results for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· Stimwave Technologies Inc

Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US -...

The Issue: The product contains a non-functional component not in product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· Stimwave Technologies Inc

Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model FR4A-TRL-AO US -...

The Issue: The product contains a non-functional component not in product labeling.

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

Class II — Potential Health HazardOngoing