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. 1,900 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,900 in last 12 months

Showing 2800128020 of 54,363 recalls

DrugMay 16, 2018· Ideaz Llc

Recalled Item: screamin' hot (capsaicin) Pain Relieving Gel Recalled by Ideaz Llc Due to...

The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2018· Ideaz Llc

Recalled Item: screamin' menthol (menthol) Pain Relieving Gel Recalled by Ideaz Llc Due to...

The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 16, 2018· Inopak Ltd

Recalled Item: Option Systems Antibacterial Foaming Hand Wash with .3% PCMX Recalled by...

The Issue: Microbial contamination of NonSterile Product; FDA analysis returned out of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Apolipoprotein A1 is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Correction vector...

The Issue: Correction vector confirmation message is lost if access point is changed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin M is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: C4 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: BALL TIP GUIDE WIRE 3.2MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: G-PIN 2.8BL 3.2PL 98CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: G-PIN 2.8BL 3.2PL 98CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: GUIDE WIRE w/ BALL TIP 2.0MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Elekta, Inc.

Recalled Item: HexaPOD evo RT Couch Top (also known as HexaPOD evo Module) Recalled by...

The Issue: Upon completion of a 6D workflow, the HexaPOD evo Module may be in a tilted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: DRILL PT GUIDE WIRE 3.2MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Apolipoprotein B is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin G is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: Immunoglobulin A is an in vitro diagnostic assay for the Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: G-PIN 2.8BL 3.2PL 60CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: 3.2MM X 510MM COCR THD TIP Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: BEAD TIP GD WIRE 3.0MM X 60CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: DRILL PT GUIDE WIRE 2MM X 60CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing