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. 1,887 recalls have been distributed to North Carolina in the last 12 months.
Showing 28461–28480 of 29,737 recalls
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling
The Issue: The product may mislabel patient information on culture specimen bottles due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan Recalled by Toshiba...
The Issue: It was found that there is a problem with the LCD monitor used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare - Giraffe and Panda T-Piece Resuscitation System The Recalled...
The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invivo Corporation Expression MRI Patient Monitoring System. The Expression...
The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe and Panda Bag and Mask Resuscitation System The T-piece Recalled by...
The Issue: Oxygen and air wall inlet fittings on the back panel of the resuscitation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral Recalled...
The Issue: OSSUR is recalling the Symbionic Leg because it is not recognizing the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Large External Fixation Recalled by Synthes USA HQ, Inc. Due to It...
The Issue: It was discovered internally that there was a discrepancy between the insert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler Set Single Conn. Ext. DL. Part Number: Recalled by...
The Issue: There is a small risk of a leak in Cycler Sets and if the Cycler Set is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Discovery NM/CT670 Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Enteralite Ambulatory Feeding Pumps Recalled by MOOG Medical...
The Issue: The firm is adding an addendum to the operator's manual for Infinity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS AmpliPrep Instrument (CAP) with AMPLILINK (AL) Software v.3.3.5...
The Issue: Certain COBAS AmpliPrep instruments using AMPILINK software v.3.3.4 had the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Stryker Model 6390 Recalled by Stryker Medical Division of Stryker...
The Issue: Model 6390 Power-LOAD systems built between September 12, 2012 and September...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens StreamLAB(R) Analytical Workcell Recalled by Siemens Healthcare...
The Issue: Firm has received reports from customers that the small pins at the bottom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilette Mira Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a risk of lost images during examination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.