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 55415560 of 27,512 recalls

Medical DeviceSeptember 8, 2023· GE Medical Systems China Co., Ltd.

Recalled Item: F2-01 Frame Recalled by GE Medical Systems China Co., Ltd. Due to There is a...

The Issue: There is a potential interruption of data communication between E-modules...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2023· Blue Belt Technologies, Inc

Recalled Item: Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software...

The Issue: CORI software was missing a planning stage that appears in cases of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Beckman Coulter Biomedical Division

Recalled Item: AU/DxC AU Chemistry Transferrin Immune complexes formed in Recalled by...

The Issue: The firm has identified that the Transferrin reagent does not meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000 Recalled by...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000 Recalled by...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Imola-IVD Clinical Chemistry Analyzer Catalog Number: RX4900. RX4900R ()...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number:...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Randox Laboratories Ltd.

Recalled Item: RX Daytona Plus (without ISE)- IVD Clinical Chemistry Analyser (1) RX4041...

The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. W/O CDX BLUESTAR Recalled by Fresenius Medical Care Holdings,...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis SYS Recalled by Fresenius Medical Care Holdings, Inc. Due...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. W/O CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis System w/Bibag Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T GEN 2 Bibag without CDX Recalled by Fresenius Medical Care Holdings,...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis System without CDX Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis CII Safe ES Recalled by CareFusion 303, Inc. Due to When global...

The Issue: When global edit is used to update multiple formulary properties...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. CDX BLUESTAR Recalled by Fresenius Medical Care Holdings, Inc....

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· GE MEDICAL SYSTEMS, ISRAEL LTD.

Recalled Item: Venue Go Standard Carts Ref: (H45181VC and H45103VCW) Recalled by GE MEDICAL...

The Issue: Some Venue Go Standard Carts can develop an internal failure of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Getinge Usa Sales Inc

Recalled Item: Meera Mobile Operating Table-to support and position the patient immediately...

The Issue: Under certain conditions, an issue might prevent the device from performing...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2023· Mazor Robotics Ltd

Recalled Item: MAZOR X robotic guidance system Recalled by Mazor Robotics Ltd Due to...

The Issue: Software update

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

Class II — Potential Health HazardOngoing