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. 2,363 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,363 in last 12 months

Showing 2626126280 of 27,512 recalls

Medical DeviceOctober 25, 2012· Verathon, Inc.

Recalled Item: The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that...

The Issue: Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2012· Kerr Corporation

Recalled Item: BioPlant Recalled by Kerr Corporation Due to The firm initiated the recall...

The Issue: The firm initiated the recall becaue disturbing the BioPlant product soon...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Philips Healthcare Inc.

Recalled Item: Philips DigitalDiagnost X-Ray System with Eleva Software 2.1.3 Model numbers...

The Issue: When the operator for a wall stand view selects an "image rotation"...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Hoffman LRF Wire Bolt Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Two complaints have been filed where Hoffman LRF Wires have broken during...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Baby Quasar (LAB-001-D Recalled by Quasar Bio-Tech, Inc. dba Silver Bay LLC...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Sekisui Diagnostics Llc

Recalled Item: Sekisui Diagnostics Recalled by Sekisui Diagnostics Llc Due to Spectrolyse...

The Issue: Spectrolyse PAI-1 activity assay, producing lower than expected absorbance...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: B. Braun Medical Inc. has become aware of an issue with the Outlook ES...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing