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. 1,042 recalls have been distributed to North Carolina in the last 12 months.
Showing 20461–20480 of 54,363 recalls
Recalled Item: Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp Recalled by Advanced...
The Issue: Firm testing found Vibrio parahaemolyticus in cooked butterfly shrimp from...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sprout Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mixed Greens 4 oz. Product contains red clover sprouts. Recalled by Chicago...
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spring Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...
The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PreludeSYNC DISTAL Radial Compression Devices Recalled by Merit Medical...
The Issue: During the sterilization of radial compression devices, some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to...
The Issue: Updated Instructions For Use- to contraindications and potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...
The Issue: CGMP Deviations: Presence of dark brown discoloration on edges of tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Probe Recalled by Northgate Technologies, Inc. Due to As part of an...
The Issue: As part of an investigation into a biocompatibility test discrepancy where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product...
The Issue: Intermittent failure of a signal being sent to a monitor from the touch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 FLEX Recalled by Radiometer Medical ApS Due to Analyzer's barcode...
The Issue: Analyzer's barcode reader misinterprets the contents of barcode label used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOLITH URO-TCH 9FR PROBE 54CM Recalled by Northgate Technologies, Inc. Due...
The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies...
The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products TT4 Reagent Pack Recalled by Ortho Clinical...
The Issue: The specified reagent packs exhibit an increase in the frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom convenience kits containing Medline brand Sterile Pre-Saturated...
The Issue: Medline identified that there may be a potential for voids in the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The CF-70 instrument (product code: LXG Recalled by Sysmex America, Inc. Due...
The Issue: Software mismatch-When the software versions between the SP-50 and CF-70 are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuflex Plus Ureteral Stent Set 7FX24CM with .035 Sensor UPN: Recalled by...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuflex Plus Ureteral Stent Set 6FX24CM with .038 Sensor UPN: Recalled by...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .035 3CM FLEX STR/150CM Recalled by...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stretch VL Ureteral Stent Set 7FX22-30CM with .035 Sensor UPN: M006185157080...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stretch VL Ureteral Stent Set 4.8FX22-30CM with .035 Sensor UPN:...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.