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. 2,547 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,547 in last 12 months

Showing 54615480 of 47,938 recalls

Medical DeviceMay 13, 2024· Young Dental Manufacturing I, LLC

Recalled Item: Darby Prophylaxis Paste with 1.23% Fluoride Ion Recalled by Young Dental...

The Issue: Part number 040032, Lot number, 248607 was incorrectly labeled as part...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· SIGHT DIAGNOSTICS LTD

Recalled Item: Sight OLO CBC Test Kit Recalled by SIGHT DIAGNOSTICS LTD Due to One Test Kit...

The Issue: One Test Kit lot (TK1-10114) shows a positive bias in the platelet count due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· Draeger Medical Systems, Inc.

Recalled Item: Infinity Acute Care System (IACS) Monitoring System Recalled by Draeger...

The Issue: Device is not in full compliance to Type CF requirements of IEC 60601-1 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...

The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· Aesculap Inc

Recalled Item: Aeos Robotic Digital Microscope Recalled by Aesculap Inc Due to Possibility...

The Issue: Possibility of the robotic arm to drop more than 10cm from its original...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2024· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in...

The Issue: The reason for recall is the meters may show an incorrect measurement unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: MONOCRYL (poliglecaprone 25) Suture - Intended for use in general Recalled...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Beaver Visitec International, Inc.

Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...

The Issue: The wrong configuration of the blade was in the package. The bevel was on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 - Designed to Recalled by Ion Beam...

The Issue: Irradiation is not interrupted when some C230 Accelerator Control Unit...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: VICRYL (polyglactin 910) Suture - Indicated for use in general Recalled by...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: MONOCRYL Plus Antibacterial (poliglecaprone 25) Suture - Intended for use...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: PDS II (polydioxanone) Suture - Intended for use in general Recalled by...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in Recalled...

The Issue: Issue on a specific packaging machine resulted in a hole in the primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2024· Beaver Visitec International, Inc.

Recalled Item: Xstar Safety Slit Knife Recalled by Beaver Visitec International, Inc. Due...

The Issue: The wrong configuration of the blade was in the package. The bevel was on...

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

Class II — Potential Health HazardOngoing
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back Label states Each contains:...

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back label states Each contains:...

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Rizatriptan Benzoate Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back Label states 'Each contains:...

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back Label states 'Each contains:...

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

Class III — Low RiskOngoing
Refund