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. 1,913 recalls have been distributed to North Carolina in the last 12 months.
Showing 26361–26380 of 54,363 recalls
Recalled Item: Genicon Natura Model 210-005-052 Recalled by Genicon, Inc. Due to There is...
The Issue: There is potential for the plastic optical tip to become detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to The...
The Issue: The catheter failed the endotoxin testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECMO Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...
The Issue: These catheters may have the following deficiencies: 1) barium sulfate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Montelukast Sodium Tablets Recalled by Hetero Labs Limited Unit V Due to...
The Issue: Discoloration: A complaint was received from a pharmacist for the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VitalBeam Radiotherapy Delivery System Version 2.5 Product Usage: The...
The Issue: Reports have been received of an anomaly that can result in a treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical 14" (36 cm) Appx 3.6 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Design change implemented changing the device from a blood set with a filter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy...
The Issue: Reports have been received of an anomaly that can result in a treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amlodipine and Valsartan Tablets Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Valsartan Tablets Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets USP Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine and Valsartan Tablets Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets USP Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets USP Recalled by Torrent Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.