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. 1,085 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,085 in last 12 months

Showing 14921–14940 of 29,737 recalls

Medical DeviceJanuary 14, 2019· Shimadzu Medical Systems Usa Com

Recalled Item: BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is...

The Issue: Normal operation of the device is to power up the device in the morning,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2019· Teleflex Medical

Recalled Item: RUSCH Urinary Drainage bag Recalled by Teleflex Medical Due to The device...

The Issue: The device labels are not UDI compliant. The missing UDI compliance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJanuary 14, 2019· Teleflex Medical

Recalled Item: RUSCH CARE Premium Drain bag Recalled by Teleflex Medical Due to The device...

The Issue: The device labels are not UDI compliant. The missing UDI compliance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJanuary 11, 2019· AAP Implantate Ag

Recalled Item: aap Implante AG Recalled by AAP Implantate Ag Due to There is the potential...

The Issue: There is the potential for the Lambotte chisel to break at the welded piece...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2019· Lin-Zhi International Inc

Recalled Item: Ethyl Alcohol Enzymatic Assay Recalled by Lin-Zhi International Inc Due to...

The Issue: Shelf life of the product may be reduced due to degradation of the assay.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJanuary 10, 2019· Arrow International Inc

Recalled Item: Arrow¿ Two-Lumen Central Venous Catheterization Set with Blue FlexTip¿...

The Issue: The product lidstock contains a labelling error. The lidstock states the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: AutoDELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y15 MagValve Product Usage: The PushValves/ MagValves is intended...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: DELFIA¿ hCG Kit Recalled by PerkinElmer Life and Analytical Sciences,...

The Issue: hCG analyte concentrations may be decreased up to 15- 20% at the lower...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Ottobock Orthopedic Industrie

Recalled Item: 21Y14 PushValve Product Usage: The PushValves/ MagValves is intended...

The Issue: Some of the installed valve-inserts have a diameter smaller than the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Bio-Rad Laboratories, Inc

Recalled Item: EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management...

The Issue: User-induced circumstances can contribute to the EVOLIS Microplate Processor...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2019· Arrow International Inc

Recalled Item: Arrow¿ Two-Lumen Central Venous Catheterization Kit with Blue FlexTip¿...

The Issue: The product lidstock contains a labelling error. The lidstock states the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC30 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Feeding Tube Metric Recalled by ConvaTec, Inc Due to An internal assessment...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: Nelaton Urinary Catheter Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· ConvaTec, Inc

Recalled Item: FilterFlow Suction Handle CH24 Recalled by ConvaTec, Inc Due to An internal...

The Issue: An internal assessment of packaging confirmed the potential for a breach in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC70 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2019· Philips North America, LLC

Recalled Item: PageWriter TC50 Recalled by Philips North America, LLC Due to Philips...

The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing