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 52941–52960 of 54,363 recalls
Recalled Item: syngo Dynamics Version 9.5 Recalled by Siemens Medical Solutions, USA, Inc...
The Issue: If multiple uncompressed images/clips are sent to the syngo Dynamics server,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESSORY BASE STARTER KIT Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOMIX High Speed Compounder System Recalled by Baxter Healthcare Corp. Due...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage TOX Drug Screen 9 Panel Recalled by Alere San Diego, Inc. Due...
The Issue: Alere San Diego is recalling Alere Triage TOX Drug Screen because there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD Recalled...
The Issue: The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a number of potential issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Hot Salsa Recalled by Pulmuone...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa - Canada (containing...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Mild Salsa Recalled by Pulmuone...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa Recalled by Pulmuone...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Emerald Valley Kitchen Organic Medium Salsa - Canada (containing...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Organic Medium Salsa Recalled by Pulmuone Wildwood Inc Due to The...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wildwood Organic Mild Salsa Recalled by Pulmuone Wildwood Inc Due to The...
The Issue: The firm recalled due to a potential non-safety quality concern related to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Transdermal System Recalled by Actavis Due to Subpotent; some...
The Issue: Subpotent; some patches may not contain fentanyl gel
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ventlab Premium Small Adult Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.