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. 1,004 recalls have been distributed to North Carolina in the last 12 months.
Showing 30721–30740 of 54,363 recalls
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Succinylcholine Chloride Injection (Preserved) 20 mg per mL Recalled by...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 15 mMol in Recalled by...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 20 mMol in Recalled by...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cobalt MV with Gentamicin Recalled by Encore Medical, Lp Due to Loss of the...
The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere iScreen Dx Urine Drug Screen Card Recalled by Ameditech Inc Due to The...
The Issue: The kit box label incorrectly identifies PCP (instead of TCA) as one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectra-System/Legacy Guided Surgery Handle Kit Recalled by Implant Direct...
The Issue: The inside diameter of the 2.3mm small drill guide inserts have a smaller...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt HV Bone Cement 40GM Recalled by Encore Medical, Lp Due to Loss of the...
The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt HV with Gentamicin Recalled by Encore Medical, Lp Due to Loss of the...
The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20 Recalled by Stryker...
The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt MV Bone Cement 40GM Recalled by Encore Medical, Lp Due to Loss of the...
The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.