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. 2,763 recalls have been distributed to North Carolina in the last 12 months.
Showing 11261–11280 of 54,363 recalls
Recalled Item: Luminos dRF with software VD10- A diagnostic imaging system for Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Qualitative assay for use on Recalled by...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B Qualitative nucleic acid test for Recalled...
The Issue: The firm received customer complaints regarding false negative Influenza A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia Max with software VE10 & VF11- A diagnostic Recalled by...
The Issue: Potential risk of collision with the ceiling, wall, or objects which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELAY PRO Recalled by Bolton Medical Inc. Due to The product may be shorter...
The Issue: The product may be shorter than packaging indicates
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CustomEyes kits Recalled by Beaver Visitec International, Inc. Due to Device...
The Issue: Device packaging may contain open seals, compromising product sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultracell Wick with 80cc Collection Bag Recalled by Beaver Visitec...
The Issue: Device packaging may contain open seals, compromising product sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifampin Capsules USP Recalled by Amerisource Health Services LLC Due to...
The Issue: Failed Impurities/Degradations Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alsultan Sweets Betefour 10.5oz (600 grams) Recalled by FALCON IMPORT &...
The Issue: Undeclared cashews, almonds, and pistachios
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alsultan Sweets Mixed Baklava 12.3oz (350 grams) /750 grams Recalled by...
The Issue: Undeclared milk and wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scan Monitor/ScanWatch Recalled by Withings Due to A software bug eliminated...
The Issue: A software bug eliminated the initial ECG activation and review of the ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: The Cardiosave IABP may shut down unexpectedly due to blood entering in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOSTOP G BIORESORBABLE CEMENT RESTRICTOR Catalog Numbers: 546308000 (Size...
The Issue: All lots of BIOSTOP G Bioresorbable Cement Restrictor are being removed as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Nuclear Medicine 600/800 series systems Recalled by GE MEDICAL SYSTEMS...
The Issue: A mitigation may not be correctly implemented. If this is the case, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.