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. 2,005 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,005 in last 12 months

Showing 1202112040 of 54,363 recalls

Medical DeviceSeptember 30, 2022· Boston Scientific Corporation

Recalled Item: EMBLEM S-ICD Recalled by Boston Scientific Corporation Due to There is an...

The Issue: There is an incorrect manufacturing date/timestamp within the software which...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE LITHOTOMY Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB EYE PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE DENTAL PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· Wright Medical Technology, Inc.

Recalled Item: Stryker INBONE Tibial Tray Recalled by Wright Medical Technology, Inc. Due...

The Issue: The tibial tray lock detail is oversized (larger than specification).

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB CATARACT PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB EYE MUSCLE Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2022· Boston Scientific Corporation

Recalled Item: EMBLEM MRI S-ICD Recalled by Boston Scientific Corporation Due to There is...

The Issue: There is an incorrect manufacturing date/timestamp within the software which...

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

Class II — Potential Health HazardOngoing
DrugSeptember 30, 2022· Ingenus Pharmaceuticals Llc

Recalled Item: Flunisolide Nasal Solution Recalled by Ingenus Pharmaceuticals Llc Due to...

The Issue: Out of specification for related substances (impurities).

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2022· VistaPharm, Inc.

Recalled Item: Pyridostigmine Bromide Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: cGMP Deviations: Out of specification for assay of one of the preservative...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2022· AuroMedics Pharma LLC

Recalled Item: Fondaparinux Sodium Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Subpotent Drug: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 30, 2022· Swiss American Inc

Recalled Item: Saint Louis Domestic Brie Wedge Recalled by Swiss American Inc Due to...

The Issue: Potential contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 29, 2022· Golden State Medical Supply Inc.

Recalled Item: Atenolol Tablets Recalled by Golden State Medical Supply Inc. Due to Label...

The Issue: Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 29, 2022· CIPLA

Recalled Item: Arformoterol Tartrate Inhalation Solution Recalled by CIPLA Due to Lack of...

The Issue: Lack of Assurance of Sterility: environmental monitoring failure.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 29, 2022· Canon Medical System, USA, INC.

Recalled Item: Canon Aplio ultrasound system Recalled by Canon Medical System, USA, INC....

The Issue: After completion, ultrasound system's Stress Echo may not terminate if user...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Kamiya Biomedical Company, LLC

Recalled Item: K-ASSAY IgA Immunoturbidimetric Assay Recalled by Kamiya Biomedical Company,...

The Issue: IgA Reagent may start showing cloudiness over time, which can affect assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Biokit, S.A.

Recalled Item: biokitHSV-2 Rapid Test Recalled by Biokit, S.A. Due to HSV-2 rapid test may...

The Issue: HSV-2 rapid test may report false positive results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing