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. 2,471 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,471 in last 12 months

Showing 1438114400 of 27,512 recalls

Medical DeviceDecember 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: When the Millipore Water Purification Module Progard Pretreatment Packs are...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 1500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: When the Millipore Water Purification Module Progard Pretreatment Packs are...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Product Usage: The Proton Therapy System - Proteus Recalled by...

The Issue: There is a risk of detachment of the Compact Gantry Rolling Floor.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Applied Medical Resources Corp

Recalled Item: GelPOINT Path Transanal Procedural Pack with Epix Electrosurgical L-Hook...

The Issue: Unintentional shifting of the tip insulation of the firm's electrosurgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Applied Medical Resources Corp

Recalled Item: Epix Electrosurgical Probes with Smoke Evacuation Recalled by Applied...

The Issue: Unintentional shifting of the tip insulation of the firm's electrosurgical...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Baxter Healthcare Corporation

Recalled Item: AMIA Automated Peritoneal Dialysis System Product Usage: It is intended...

The Issue: Potential for the software on Automated PD System cyclers which can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic...

The Issue: Negative bias results when using VITROS VALP Reagent, GEN 25.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Baxter Healthcare Corporation

Recalled Item: Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended...

The Issue: Potential for the software on Automated PD System cyclers which can cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· Signature Orthopedics Pty Limited

Recalled Item: Genius Knee Cemented Tibial Component Product Usage: Knee replacement...

The Issue: Product mix up

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· ProSun International, LLC

Recalled Item: ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed Recalled by ProSun...

The Issue: ProSun International LLC discovered discrepancies in their Quality Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· ProSun International, LLC

Recalled Item: ProSun V3 42 Xlc(160w)(10 minutes) tanning bed Recalled by ProSun...

The Issue: ProSun International LLC discovered discrepancies in their Quality Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· Signature Orthopedics Pty Limited

Recalled Item: Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement...

The Issue: Product mix up

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM aTG (500 test kit) Siemens Material Number (SMN): 10995462...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Atellica IM aTG (100 test kit) Siemens Material Number (SMN):...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Siemens Healthcare Diagnostics, Inc

Recalled Item: SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN):...

The Issue: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2018· Ethicon Endo-Surgery Inc

Recalled Item: PROXIMATE¿ HCS Hemorrhoidal Circular Stapler Product Code: PPH01 PPH01: The...

The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...

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

Class II — Potential Health HazardOngoing