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. 2,808 recalls have been distributed to North Carolina in the last 12 months.
Showing 5221–5240 of 54,363 recalls
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft Infusion Set Recalled by Unomedical A/S Due to Specific VariSoftTM...
The Issue: Specific VariSoftTM Infusion Sets were packaged using incorrect secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...
The Issue: Various medical device product IFUs contain reprocessing modalities that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glenmark Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ClotTriever XL Catheter Recalled by Inari Medical - Oak Canyon Due to...
The Issue: Thrombectomy system catheter instructions for use updated to reduce adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for Recalled by...
The Issue: May intermittently produce falsely resistant results for pyrazinamide (PZA)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...
The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...
The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective container; yellow colored spike from cap lodged in the nozzle
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Umary Acido Hialuronico Recalled by MAIN PRODUCTS INC Due to Undeclared...
The Issue: Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kenny's Farmhouse Cheese - St. Jerome packaged in plastic vacuum Recalled by...
The Issue: Potential contamination with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Power Express Recalled by Beckman Coulter Biomedical GmbH Due to The...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE Centrifuge Recalled by Beckman Coulter Biomedical GmbH Due to The...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mazor X. Model Number Recalled by Mazor Robotics Ltd Due to Software...
The Issue: Software anomalies which can result in two separate issues: A lagging screen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAVEWRITER ALPHA: Model: SC-1216 Recalled by Boston Scientific...
The Issue: Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter...
The Issue: The Spectrum WBM may fail to auto-document infusion status information back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.