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. 1,117 recalls have been distributed to North Carolina in the last 12 months.
Showing 8041–8060 of 54,363 recalls
Recalled Item: Montelukast Sodium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Presence of Foreign Tablet(s)/Capsule(s): A foreign tablet was found in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novum IQ Syringe infusion system Recalled by Baxter Healthcare Corporation...
The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...
The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp-i Recalled by Maquet Medical Systems USA Due to It was found that...
The Issue: It was found that the fixation (weld) employed by the supplier of the nut...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...
The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE Model Numbers BF-1TH190 Recalled by Olympus...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Number Q180-AC...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T150 Recalled by Olympus...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-P190 Recalled by...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-XT190 Recalled by...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...
The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T180...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...
The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline manual resuscitators with integrated manometer Recalled by SunMed...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VariSoft infusion set Recalled by Unomedical A/S Due to The Varisoft...
The Issue: The Varisoft infusion set is used in conjunction with tandem insulin pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex manual resuscitators with integrated manometer Recalled by SunMed...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventlab Recalled by SunMed Holdings, LLC Due to A backwards leak present in...
The Issue: A backwards leak present in the integrated manometer of the patient valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD gravity sets (Product Name Recalled by Becton Dickinson & Company Due to...
The Issue: Affected infusion sets labeled as free of DEHP actually do contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.