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. 992 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
992 in last 12 months

Showing 18221–18240 of 47,938 recalls

Medical DeviceMay 11, 2020· Biomet, Inc.

Recalled Item: Comprehensive VRS Inserter Recalled by Biomet, Inc. Due to The product is...

The Issue: The product is being recalled due to the central screw drill seizing inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Radiometer Medical ApS

Recalled Item: ABL80-FLEX-393-839 Box Label Recalled by Radiometer Medical ApS Due to...

The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...

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

Class II — Potential Health HazardOngoing
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Cannabidiol (CBD) 4mg/mL Recalled by BIOTA Biosciences LLC Due to...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Curcumin Recalled by BIOTA Biosciences LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Curcumin 50mg/mL Recalled by BIOTA Biosciences LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Cannabidiol (CBD) + Curcumin 50mg/mL Recalled by BIOTA Biosciences...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· Torrent Pharma Inc.

Recalled Item: Carbamazepine Tablets Recalled by Torrent Pharma Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Cannabidiol (CBD) 50mg/mL Recalled by BIOTA Biosciences LLC Due to...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 8, 2020· ICU Medical Inc

Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...

The Issue: Presence of Particulate Matter: confirmed customer complaint for the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 8, 2020· Merge Healthcare, Inc.

Recalled Item: Merge Healthcare Merge Application Server Software Release and Merge...

The Issue: An error in the calculation of the Michigan Ranges can generate an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2020· Ge Healthcare

Recalled Item: The OEC 9900 C-Arm is designed to provide fluoroscopic and Recalled by Ge...

The Issue: GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap T2 Tibia +10 mm Catalog Number: 18220010S Recalled by...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker End Cap Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: MAMMOMAT Revelation Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If an examination is interrupted when the InSpect Projection View (PV) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2020· Stryker GmbH

Recalled Item: Stryker Locking Screw Recalled by Stryker GmbH Due to Seal integrity of the...

The Issue: Seal integrity of the blister pack may be compromised and sterility cannot...

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

Class II — Potential Health HazardOngoing