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 2536125380 of 27,512 recalls

Medical DeviceMay 10, 2013· Symbios Medical Products, LLC

Recalled Item: Part 510180 Disposable Single Infusion Pump Recalled by Symbios Medical...

The Issue: Symbios Medical Products, Indianapolis, Indiana, is performing a voluntary...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: Dimension Vista System TSH Flex Reagent Cartridge (). Intended Recalled by...

The Issue: A rare variant of TSH, identified in a small cluster of patients, is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CRP Slides (Reagent) Recalled by Ortho-Clinical...

The Issue: While performing interval testing Ortho Clinical Diagnostics (OCD)...

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

Class III — Low RiskOngoing
Medical DeviceMay 9, 2013· Integra LifeSciences Corporation

Recalled Item: Integra PANTA Arthrodesis Nail System. Intended for use in...

The Issue: As a result of the investigation into an adverse trend of complaints for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2013· ConBio, a CynoSure Company

Recalled Item: Multilite Dye Handpieces Recalled by ConBio, a CynoSure Company Due to An...

The Issue: An inconsistency was identified related to electronic display identification...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products K+ (Potassium) Slides (Reagent) Recalled by...

The Issue: While performing interval testing, Ortho Clinical Diagnostics (OCD)...

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

Class III — Low RiskOngoing
Medical DeviceMay 9, 2013· Novarad Corporation

Recalled Item: NovaPACS  versions 7.4 Recalled by Novarad Corporation Due to Potential for...

The Issue: Potential for images to be flipped while streaming, which could incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8 mm Monopolar Curved Scissors (a.k.a. Hot Shears) Manufactured and Recalled...

The Issue: Intuitive Surgical has identified a potential for some units of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Maryland Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Precise Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· Intuitive Surgical, Inc.

Recalled Item: 8mm Fenestrated Bipolar Forceps used in conjunction with the da Recalled by...

The Issue: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2013· DePuy Orthopaedics, Inc.

Recalled Item: DePuy LifeLiner Stick & Cut Resistant Gloves Rt Recalled by DePuy...

The Issue: LifeLiner Stick and Cut Resistant Gloves are being recalled because cases...

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

Class III — Low RiskOngoing
Medical DeviceMay 8, 2013· Verathon, Inc.

Recalled Item: GlideScope Video Laryngoscope (GVL) 3 Recalled by Verathon, Inc. Due to...

The Issue: Verathon GlideScope Reusable GVL and AVL Blades are being recalled due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: The Zimmer Air Dermatome Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· SpineFrontier, Inc.

Recalled Item: InSpan Inserter Recalled by SpineFrontier, Inc. Due to Potential for set...

The Issue: Potential for set screw to be come deformed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2013· Zimmer Surgical Inc

Recalled Item: Zimmer Air Dermatome II Recalled by Zimmer Surgical Inc Due to This removal...

The Issue: This removal is in response to complaints alleging that the Zimmer Air...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens RAD Fluoro Uro Systems - Luminos dRF Recalled by Siemens Medical...

The Issue: Siemens has discovered through product monitoring a potential malfunction...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Alphatec Spine, Inc.

Recalled Item: Leucadia Autolok" Polyaxial Pedicle Screw System. Intended to help provide...

The Issue: Alphatec Spine initiated this medical device recall for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2013· Covidien LP

Recalled Item: Versaport Bladeless Optical Fixation Cannula - 5mm Product Code: ONBFCA5ST...

The Issue: Seals may disengage from the cannula which may result in a component...

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

Class II — Potential Health HazardOngoing