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. 1,117 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,117 in last 12 months

Showing 10161–10180 of 29,737 recalls

Medical DeviceMarch 18, 2021· Luminex Corporation

Recalled Item: VERIGENE Processor SP - Product Usage: intended for processing and Recalled...

The Issue: Potential for a false-negative result for Vibrio parahaemolyticus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaBplus and AquaBplus B2 Water Purification System - Product Usage:...

The Issue: AquaBplus HF module on the AquaBplus 2500 osmosis system, an error in the US...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Integra LifeSciences Corp.

Recalled Item: CODMAN HAKIM BACTISEAL Shunt System Clear with Barium Stripe Peritoneal...

The Issue: Incorrect labeling, Catheter did not have the required holes and markings

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Clark Laboratories, Inc.

Recalled Item: Trinity Biotech Captia Measles IgM Kit Recalled by Clark Laboratories, Inc....

The Issue: Positive Control may run high out of its assigned ISR range and result in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Medtronic Sofamor Danek USA, Inc

Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...

The Issue: The shelf box identifies a small device actually contains a large device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Becton Dickinson & Co.

Recalled Item: BD BBL Martin-Lewis Agar Recalled by Becton Dickinson & Co. Due to Products...

The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Medtronic Sofamor Danek USA, Inc

Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...

The Issue: The shelf box identifies a small device actually contains a large device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Becton Dickinson & Co.

Recalled Item: BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use Recalled by Becton...

The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· SIGHT DIAGNOSTICS LTD

Recalled Item: Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #:...

The Issue: Discrepancy in labeling between the adult CBC ranges presented in the OLO...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Boston Scientific Corporation

Recalled Item: EXALT Controller - Product Usage: intended for use with a Recalled by Boston...

The Issue: May have been programmed with a less than optimal brightness setting...

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

Class III — Low RiskOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port Recalled by...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 60mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Due to...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.3 mL Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/60" (152 cm) Appx 2.2 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628 Recalled by...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: Oncology Kit w/Spiros¿ Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· ICU Medical, Inc.

Recalled Item: 5 IN (13cm) APPX 0.57 ml Recalled by ICU Medical, Inc. Due to Due to molding...

The Issue: Due to molding defect, there is a potential that certain lots of spinning...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2021· Cardinal Health Inc.

Recalled Item: FREESTYLE LANCETS 28G 100CT Item Number:2975670 Recalled by Cardinal Health...

The Issue: Due to shipping delays the devices were exposed to temperature excursions of...

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

Class II — Potential Health HazardOngoing