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. 1,932 recalls have been distributed to North Carolina in the last 12 months.
Showing 17141–17160 of 29,737 recalls
Recalled Item: SOMATOM Emotion 16 (10165977) Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Spirit(Model 10045692 ) Recalled by Siemens Medical Solutions USA,...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline 0.9 % Sodium Chloride Injection Recalled by Medline Industries Inc...
The Issue: Packaged with an incorrect overwrap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Ambulatory EEG Recalled by Natus Neurology Inc Due to Potential to...
The Issue: Potential to be able to import an ambulatory exam for a patient for which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Exhaust Cap Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Exhaust Line Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Probe Cap Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker C02 Cartridge Recalled by Cook Inc. Due to The interior of the...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Pneumatic Lithotripter Recalled by Cook Inc. Due to The...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Sterilization Cap Recalled by Cook Inc. Due to The interior of...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StoneBreaker Single Use Probe Recalled by Cook Inc. Due to The interior of...
The Issue: The interior of the product may not be sterilized to the appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: Broken or missing screws and retaining clips. This may be due to screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Calcium Flex¿ reagent cartridge Recalled by Siemens...
The Issue: May produce erroneously low results from specific well sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Revision Knee Catalog #5545-A-301 and Catalog #5546-A-601 The knee...
The Issue: Customers may receive the incorrect size implant from what is labeled on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...
The Issue: The device could have a missing spanner nut and snap ring which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips QCPR Meter - used with FR3 Product Usage: The Recalled by Philips...
The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips QCPR Meter - used with MRx Product Usage: The Recalled by Philips...
The Issue: Inform users of correct placement of the disposable adhesive pad on the QCPR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altivate Anatomic(TM) INSTRUMENTATION Recalled by Encore Medical, Lp Due to...
The Issue: It was discovered during a surgery that the design of the radius at the base...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.