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. 2,828 recalls have been distributed to North Carolina in the last 12 months.
Showing 1581–1600 of 54,363 recalls
Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Unichem Pharmaceuticals...
The Issue: Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% SODIUM CHLORIDE IRRIGATION USP. ISOTONIC SOLUTION FOR IRRIGATION...
The Issue: Lack of Assurance of Sterility- Potential for fluid leakage from the port...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STERILE WATER FOR INJECTION USP Recalled by B BRAUN MEDICAL INC Due to Lack...
The Issue: Lack of Assurance of Sterility- Potential for fluid leakage from the port...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GORE ACUSEAL Vascular Graft Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Reports of vascular graft delamination, which may lead to reduced access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TopCare Health 70% Isopropyl Alcohol Recalled by Consumer Product Partners,...
The Issue: Cross Contamination with Other Products.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kroger 70% Isopropyl Alcohol Recalled by Consumer Product Partners, LLC Due...
The Issue: Cross Contamination with Other Products.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chloroproMAZINE Hydrochloride Tablets Recalled by AvKARE Due to Presence of...
The Issue: Presence of a foreign substance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chloroproMAZINE Hydrochloride Tablets Recalled by AvKARE Due to Presence of...
The Issue: Presence of a foreign substance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultra Violette Mini SPF Mates kit includes: Velvet Screen SPF Recalled by...
The Issue: Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultra Violette Recalled by GRACE & FIRE PTY LTD Due to...
The Issue: Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAC VU360 Acquisition Trunk Cable and Module Holder Recalled by GE Medical...
The Issue: If a user incorrectly places the Acquisition Module into the Acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyDay Toric Recalled by CooperVision, Inc. Due to One lot manufactured with...
The Issue: One lot manufactured with an invalid sterilization cycle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyant 1-Day Premium Toric Recalled by CooperVision, Inc. Due to One lot...
The Issue: One lot manufactured with an invalid sterilization cycle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofmed Breathables Recalled by CooperVision, Inc. Due to One lot...
The Issue: One lot manufactured with an invalid sterilization cycle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Kits: 1) VALVE PACK-LF Recalled by Medline Industries, LP Due to The...
The Issue: The kits contain certain lots of cannula products where the catheter may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venclose digiRF Generators Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Software version 3.35 of the Venclose digiRF Generator incorporates a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG6+ cartridge. List Number: 03P77-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG4+ cartridge (white). List Number: 03P85-25. Recalled by Abbott...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.