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 8501–8520 of 54,363 recalls

DrugAugust 17, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL Recalled by Central...

The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: PHENYLephrine added to 0.9% sodium chloride 50 mg/250mL (200mcg/mL) Recalled...

The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...

The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: PHENYLephrine Recalled by Central Admixture Pharmacy Services, Inc. Due to...

The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: dilTIAZem 125mg/125mL (1 mg/mL) Recalled by Central Admixture Pharmacy...

The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: Neonatal TPN Starter Bag Recalled by Central Admixture Pharmacy Services,...

The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2023· Central Admixture Pharmacy Services, Inc.

Recalled Item: CARDIOPLEGIA SOLUTION Recalled by Central Admixture Pharmacy Services, Inc....

The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 17, 2023· Impedimed Limited

Recalled Item: SOZO Bilateral Arm L-Dex Software Recalled by Impedimed Limited Due to...

The Issue: Bilateral L-Dex assessment software does not have the same level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2023· Philips North America Llc

Recalled Item: Patient Information Center iX with Software Version Number 4.x in Recalled...

The Issue: Patient Information Center (PIC iX) Release 4.x Surveillance Crash Caused by...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2023· Exocad GmbH

Recalled Item: exoplan version 3.1 Rijeka Software -A medical software Recalled by Exocad...

The Issue: A software library filtering error has been discovered which occurs when...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure pack: Presource PBDS Cat. PLMHCSBHF Recalled by Cardinal Health...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure pack: Presource PBDS Recalled by Cardinal Health 200, LLC Due to...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource Pain Tray Recalled by Cardinal Health 200,...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Cat. PN33BPCR2 Recalled by Cardinal...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Presource Fistulogram Pack Recalled by Cardinal Health 200, LLC Due to Packs...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

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

Class II — Potential Health HazardOngoing