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. 1,744 recalls have been distributed to North Carolina in the last 12 months.
Showing 49481–49500 of 54,363 recalls
Recalled Item: Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution)...
The Issue: Presence of foreign substance: One lot of the product may contain black...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose...
The Issue: Research Use Only (RUO) parameters were included in TEG 5000 User Manual.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxyphen XR Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RED VIPERS Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PHEnFX (TM) Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PHENTALENE (TM) Recalled by Beta Labs Due to The products contain DMAA, also...
The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252...
The Issue: Light Image O-Spots Dispenser mislabeled as Soft n' Stretchy Light Image S-Spots
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmBisome (amphotericin B) liposome for injection Recalled by Astellas Pharma...
The Issue: Lack of Assurance of Sterility; Astellas Pharma US, Inc. is performing a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Suction Wand Recalled by Edwards Lifesciences, LLC Due...
The Issue: Edwards is recalling certain lots of Rigid Suction Wands because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Healthcare...
The Issue: The MRx may deliver a non-synchronized cardioversion shock resulting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System. The...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Tube/Plate Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. is conducting a recall for the Column end Cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX FEMORAL FIXATION SYSTEM COMPRESSION LAG SCREW Recalled by Zimmer,...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Free Lock Femoral Hip Fixation System Compression Lag Screw . Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Recalled by...
The Issue: Siemens is conducting a field correction for Dimension Vista 500 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Recalled by Hospira Inc. Due to Hospira has received reports of...
The Issue: Hospira has received reports of customers experiencing air-in-line alarms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHAMPION Medical Recliner Recalled by Invacare Corporation Due to There is a...
The Issue: There is a possibility of elevated temperatures in the seat pad. In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.