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. 1,085 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,085 in last 12 months

Showing 14261–14280 of 54,363 recalls

Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: Pain Tray Catalog Number: 9883 Recalled by Busse Hospital Disposables, Inc....

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: SS 4.5MM Pellet Insertion Tray Catalog Number:B8128R1 Recalled by Busse...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: SS 4.5MM DIAMOND TIP TROCAR WITH MEDIUM GLOVES Catalog Number: B1560...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: Single Shot Epidural Tray Catalog Number: 8417 Recalled by Busse Hospital...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: Nerve Block Tray Catalog Number: 8415 Recalled by Busse Hospital...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: Female SS 3.5MM Pellet Insertion Tray Catalog Number: B1568 Recalled by...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2022· Busse Hospital Disposables, Inc.

Recalled Item: 3.2MM Pellet Insertion Tray Catalog Number: B9743 Recalled by Busse Hospital...

The Issue: Busse Convenience kits contain one or more swab/swabstick drug products,...

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

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2022· American Health Packaging

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by American Health Packaging...

The Issue: Impurity failure at 0-time of the repackaged lot.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 22, 2022· Preferred Pharmaceuticals, Inc.

Recalled Item: Alprazolam Tablets Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 21, 2022· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Dexamethasone Elixir Recalled by Morton Grove Pharmaceuticals, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: higher than permissible levels...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 21, 2022· SA3, LLC

Recalled Item: Silatrix Oral Gel Polymerized Sucralfate Gel 10% (1 gm/10 gm Recalled by...

The Issue: Due to failure of microbial testing for total aerobic microbial count (TAMC).

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2022· Baxter Healthcare Corporation

Recalled Item: Liko Universal Twinbar 670 QRH Recalled by Baxter Healthcare Corporation Due...

The Issue: An incorrect center bolt was used in the assembly of the product which could...

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

Class II — Potential Health HazardOngoing
FoodFebruary 20, 2022· Vadilal Industries USA Inc.

Recalled Item: Vadilal Quick Treat Custard Apple Pulp Net Wt Recalled by Vadilal Industries...

The Issue: Product may be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 18, 2022· Wegmans Food Markets, Inc.

Recalled Item: Wegmans brand Roasted Garlic hummus Recalled by Wegmans Food Markets, Inc....

The Issue: Product may potentially contain blue plastic pieces.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 18, 2022· DNA Genotek Inc.

Recalled Item: ORAcollect RNA: ORE-100 Recalled by DNA Genotek Inc. Due to Evaporation of...

The Issue: Evaporation of stabilizing liquid reducing shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· GE Healthcare, LLC

Recalled Item: 1.5T SIGNA Excite HD Recalled by GE Healthcare, LLC Due to There is...

The Issue: There is potential for the images to be flipped left to right.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· GE Healthcare, LLC

Recalled Item: 1.5T and 3.0T SIGNA HDx Recalled by GE Healthcare, LLC Due to There is...

The Issue: There is potential for the images to be flipped left to right.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· DNA Genotek Inc.

Recalled Item: ORAcollect Dx Recalled by DNA Genotek Inc. Due to Evaporation of stabilizing...

The Issue: Evaporation of stabilizing liquid reducing shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· GE Healthcare, LLC

Recalled Item: Signa 1.5T TwinSpeed Magnetic Resonance Imaging System Recalled by GE...

The Issue: There is potential for the images to be flipped left to right.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2022· GE Healthcare, LLC

Recalled Item: SIGNA Excite 3T. Magnetic Resonance Imaging System Recalled by GE...

The Issue: There is potential for the images to be flipped left to right.

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

Class II — Potential Health HazardOngoing