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. 1,736 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,736 in last 12 months

Showing 4052140540 of 47,938 recalls

Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 2.0mm Zyphr Elite Round Fluted Bur Sterile Product Usage: Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
DrugMay 22, 2014· Aidarex Pharmaceuticals LLC

Recalled Item: Ciprofloxacin 500 mg tablets Recalled by Aidarex Pharmaceuticals LLC Due to...

The Issue: Presence of Foreign Tablets/Capsules: Tramodol 50 mg tablet has been found...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2014· Sandoz, Inc

Recalled Item: Cefpodoxime Proxetil Tablets Recalled by Sandoz, Inc Due to Presence of...

The Issue: Presence of Foreign Substance: Presence of stainless steel particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 21, 2014· Valeant Pharmaceuticals North America LLC

Recalled Item: Vasotec (enalapril maleate) tablets Recalled by Valeant Pharmaceuticals...

The Issue: Labeling: Incorrect or Missing Package Insert: Product is packaged with the...

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

Class III — Low RiskOngoing
Refund
DrugMay 21, 2014· Valeant Pharmaceuticals North America LLC

Recalled Item: Vaseretic (enalapril maleate/hydrochlorothiazide) 10/25 mg Tablets Recalled...

The Issue: Labeling: Incorrect or Missing Package Insert: Product is packaged with the...

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

Class III — Low RiskOngoing
Refund
FoodMay 21, 2014· KIND, LLC

Recalled Item: STRONG & KIND Hickory Smoked Almond Protein Bar Recalled by KIND, LLC Due to...

The Issue: The firm is recalling all lots of the following products due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 21, 2014· KIND, LLC

Recalled Item: STRONG & KIND Honey Smoked BBQ Almond Protein Bar Recalled by KIND, LLC Due...

The Issue: The firm is recalling all lots of the following products due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 21, 2014· KIND, LLC

Recalled Item: STRONG & KIND Thai Sweet Chili Almond Protein Bar Recalled by KIND, LLC Due...

The Issue: The firm is recalling all lots of the following products due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 21, 2014· KIND, LLC

Recalled Item: KIND HEALTHY GRAINS Maple Pumpkin Seed Bar Recalled by KIND, LLC Due to The...

The Issue: The firm is recalling all lots of the following products due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 21, 2014· KIND, LLC

Recalled Item: STRONG & KIND Roasted Jalapeno Almond Protein Bar Recalled by KIND, LLC Due...

The Issue: The firm is recalling all lots of the following products due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 21, 2014· KIND, LLC

Recalled Item: STRONG & KIND Honey Mustard Almond Protein Bar Recalled by KIND, LLC Due to...

The Issue: The firm is recalling all lots of the following products due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: IRK 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· Roche Diagnostics Operations, Inc.

Recalled Item: Roche MODULAR ANALYTICS EVO Serum Work Area (SWA) Recalled by Roche...

The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 8000 analyzer series Operators Manual Roche cobas Filter label:...

The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...

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: Vessel Sealer 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· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 6000 analyzer series Operators Manual Roche cobas Recalled by Roche...

The Issue: Under certain conditions loose ProCell/CleanCell aspiration tube filters may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2014· Becton Dickinson & Co.

Recalled Item: BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System...

The Issue: A portion of the BBL Crystal Enteric/Nonfermentor (E/NF) Identification kits...

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

Class III — Low RiskOngoing
Medical DeviceMay 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Natural Rubber Latex QRG for the da Vinci Standard Surgical System 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 21, 2014· Brainlab AG

Recalled Item: Navigation Spine & Trauma 3D Version 2.0 and 2.1 Is Recalled by Brainlab AG...

The Issue: Brainlab Navigation Software Spine & Trauma 3D 2.0/2.1 offers automatic...

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: Single Site US Manuals and Single Site OUS Manuals for 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