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. 1,825 recalls have been distributed to North Carolina in the last 12 months.
Showing 38201–38220 of 54,363 recalls
Recalled Item: CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes...
The Issue: Incorrect cannula of the sheath introducer (smaller than intended).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This reagent is for in vitro diagnostic use. Pax-5 (1EW) Recalled by Leica...
The Issue: The Bond" Polymer Detection and Novolink" Polymer Detection System may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQURE System Recalled by Radiometer America Inc Due to The AQURE System has...
The Issue: The AQURE System has a design error regarding sample type in which sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...
The Issue: PSA assay is not meeting the High Dose Hook Effect expectation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PharmaCaribe PulmoSal 7% Sodium chloride Recalled by Pharmacaribe llc Due to...
The Issue: Vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA SmDP Well Recalled by Phadia Ab Due to All equivocal and positive...
The Issue: All equivocal and positive results (greater or equal 7 EliA U/ml) on EliA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Macleods Pharma Usa...
The Issue: Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: APEXXX tablets Recalled by Nuway Distributors, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moog Curlin Infusion Recalled by MOOG Medical Devices Group Due to Moog is...
The Issue: Moog is recalling Curlin 4000, 6000, and PainSmart Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549420 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548640 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548370 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549510 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549380 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548490 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M005489490 (XMD Recalled...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548250 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548820 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548360 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548760 (XMD Recalled by...
The Issue: A feeding () valve leakage issue. The feeding valve appears to close...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.