Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,466 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,466 in last 12 months

Showing 1608116100 of 27,512 recalls

Medical DeviceJanuary 11, 2018· Ellex iScience, Inc.

Recalled Item: ellex I.Science iTRACK 250A Recalled by Ellex iScience, Inc. Due to...

The Issue: Sterility failure found in one of the units in the lot.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2018· Riverpoint Medical, LLC

Recalled Item: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint...

The Issue: Product is labeled with "CE", but is not yet approved in the European Union.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 4, 2018· Toshiba American Medical Systems Inc

Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...

The Issue: The power supply unit may be damaged and may fail to start up when the power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...

The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Teleflex Medical

Recalled Item: Percuvance(R) Percutaneous Shaft 29cm Recalled by Teleflex Medical Due to...

The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Radiology CT with 4.2.0 software version. Model Recalled...

The Issue: Software issues including: Software errors that may result in Extended Field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Teleflex Medical

Recalled Item: Percuvance(R) Percutaneous Shaft 36cm Recalled by Teleflex Medical Due to...

The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #'...

The Issue: Software issues including: Software errors that may result in Extended Field...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension¿ Free Thyroxine (FT4L) Flex¿ reagent cartridge Recalled by Siemens...

The Issue: The concentrations for biotin listed in the non-interfering substances...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Gastrin Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ Mass Creatine Kinase (MMB) Flex¿ reagent cartridge Recalled...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Roche Diagnostics Corporation

Recalled Item: Roche Acetaminophen assay 03255379160-HAcetaminophen (P) 20767174160- cobas...

The Issue: The previous version of method sheets for the Acetaminophen assay on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Anti HBc Recalled by Siemens Healthcare...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur¿ DHEA-SO4 Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: The concentrations for biotin listed in the non-interfering substances...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur¿ HBc IgM Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: Concentrations for the level of biotin that does not interfere is not...

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

Class II — Potential Health HazardOngoing