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. 2,801 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,801 in last 12 months

Showing 62816300 of 54,363 recalls

Medical DeviceApril 10, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore PEGASUS Tissue Processor Recalled by LEICA BIOSYSTEMS...

The Issue: Poorly processed and/or damaged biopsy tissue specimens on the device...

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

Class II — Potential Health HazardOngoing
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 9, 2024· GE Medical Systems Information Technologies Inc

Recalled Item: GE HealthCare CRITIKON ONE-CUF blood pressure cuffs Recalled by GE Medical...

The Issue: Use of the blood pressure cuffs could result in inaccurate non-invasive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Sophysa S.A.

Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...

The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Sophysa S.A.

Recalled Item: The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit...

The Issue: An increase in claims related to leakage of cerebrospinal fluid (CSF) from...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· QUIDELORTHO

Recalled Item: VITROS Immunodiagnostic Products Free T3 Calibrators-IVD are for use with...

The Issue: Free T3 Calibrators used with T3 Reagent Packs may produce positively biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· Baxter Healthcare Corporation

Recalled Item: Spectrum IQ Infusion pump Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential for cracks on the mount of the front panel of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2024· QUIDELORTHO

Recalled Item: VITROS Immunodiagnostic Products Free T3 Reagent Pack-IVD is for the...

The Issue: T3 Reagent Packs used with Free T3 Calibrators may produce positively biased...

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

Class II — Potential Health HazardOngoing
DrugApril 8, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Sapropterin Dihydrochloride Powder for Oral Solution 100mg Recalled by Dr....

The Issue: Sub-potent Drug; powder discoloration associated with decreased potency

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 8, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Javygtor (sapropterin dihydrochloride) Powder for Oral Solution 100mg...

The Issue: Sub-potent Drug; powder discoloration associated with decreased potency

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) NEPHROLOGY PACK Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 Recalled by...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) CONTINUOUS BLOCK Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: Novalung sensor box is a component of the Novalung Console Recalled by...

The Issue: Issue related to Novalung sensor box, which is a component of the Novalung...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2024· HeartSine Technologies Ltd

Recalled Item: HeartSine samaritan PAD (Public Access Defibrillator) Recalled by HeartSine...

The Issue: Automated external defibrillators have a manufacturing issue that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2024· Vyaire Medical, Inc.

Recalled Item: Vyaire Medical GmbH Recalled by Vyaire Medical, Inc. Due to Potential of the...

The Issue: Potential of the nozzle separating during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 5, 2024· Jiangsu Shenli Medical Production Co., Ltd.

Recalled Item: Brand Name: GMAX Product Name: SYR 5ML/LL syringe Model/Catalog Number:...

The Issue: Piston syringes sizes and configurations are out of the range of devices...

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

Class II — Potential Health HazardOngoing