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

47,938 total recalls
929 in last 12 months

Showing 40541–40560 of 47,938 recalls

Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Vessel Sealer QRG for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Cautery QRG for the da Vinci Standard Surgical System Recalled by Intuitive...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Vision Troubleshooting Guide for the da Vinci Standard Surgical System...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Insert for IRK for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Stapler Addendum for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Connection QRG for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: System Manual for the da Vinci Standard Surgical System Recalled by...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Endowrist Instrument and Accessory Manual for the da Vinci Standard Recalled...

The Issue: Multiple updates to User Manuals, Instructions for Use (IFU), Quick Guides...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: Hair Restoration Pack- Recalled by Customed, Inc Due to Customed has...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· SCC Soft Computer

Recalled Item: SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory...

The Issue: The interface fails to send abnormal flags for Lab test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ORTHO PACK EXTREMITY CUSTOMED CONTENTS: (1) TABLE COVER REINFORCED 50"...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAP Abdom w/pouch Customed code 900-2619 Recalled by Customed, Inc Due to...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: E..N.T. PACK - (5) SPONGE TONSIL 7/8 XRD (1) TABLE Recalled by Customed, Inc...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: Laparotomy Pack Recalled by Customed, Inc Due to Customed has determined...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAPAROSCOPY COLORECTAL SURGICAL PACK code 900-2259A Recalled by Customed,...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAPAROSCOPY PACK- - (1) DRAPE LAP ABDOMINAL WITH POUCH (1) Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ARTHROSCOPY PACK I (1) CUSTOMED CONTENTS: (1) TOWELS ABSORBENT 15" Recalled...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: PEDIATRIC LAP PACK - ( I) SHEET MINOR LAP 102" Recalled by Customed, Inc Due...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: PREMIUM OPHTHALMIC PACK- CUSTOMED- (1) GOWN SMS X-LARGE STD RAGLAN Recalled...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: FOLEY CATHETER KIT 1116FR. - CUSTOM ED- (1) WRAPPER 24" Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing