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. 2,808 recalls have been distributed to North Carolina in the last 12 months.
Showing 4701–4720 of 29,737 recalls
Recalled Item: ARROW QuickFlash Radial Artery Catherization (wire Recalled by ARROW...
The Issue: Teleflex is initiating this voluntary recall for the above-mentioned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a Recalled...
The Issue: Endotracheal Tube Holder included in certain kits is not compatible with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preat Nobel Active/Conical-compatible RP Titanium Blank Recalled by Preat...
The Issue: Due to a manufacturing issue, the screw seat location on the abutment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK Non-DEHP Solution Set Luer Lock Adapter Recalled by Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microStar Reader Recalled by Landauer Due to Permanent discontinuance of the...
The Issue: Permanent discontinuance of the microSTARii medical dosimetry system....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Total T4 Recalled by Beckman Coulter, Inc. Due to Four lots of Access...
The Issue: Four lots of Access Total T4 reagent lots demonstrated imprecision outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: UNclog Eye Mask Product Name: UNclog Eye Mask Recalled by EYE...
The Issue: Due to a change in the safety clips for the heated eye masks, the wires to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: natus neurology Recalled by Natus Neurology Inc Due to Natus has become...
The Issue: Natus has become aware that its third-party supplier Parker Laboratories...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Substrate Recalled by Beckman Coulter, Inc. Due to On 07 February...
The Issue: On 07 February 2024 Beckman Coulter made the decision to conduct a field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DCA Systems HbA1c Reagent Kit Recalled by Siemens Healthcare Diagnostics,...
The Issue: The reason for the recall is that the Siemens DCA HbA1c Reagent Kit was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENSIVE Conductive Adhesive Gel Recalled by Natus Neurology Inc Due to Natus...
The Issue: Natus has become aware that its third-party supplier Parker Laboratories...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP...
The Issue: When a paraPAC plus ventilator is switched to the operating mode of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP...
The Issue: When a paraPAC plus ventilator is switched to the operating mode of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent Suite Dx Software versions 5.14 and earlier used in Recalled by Life...
The Issue: Torrent Suite Dx Software versions 5.14 and earlier used in connection with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 with a Certeray generator-To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 11 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.