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. 2,404 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,404 in last 12 months

Showing 2008120100 of 27,512 recalls

Medical DeviceJanuary 29, 2016· Corin USA Limited

Recalled Item: Trinity Acetabular System Product Usage - Total Hip Replacement. Recalled by...

The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Verathon, Inc.

Recalled Item: GlideScope Titanium Single-Use Video Laryngoscope. It is a single-use video...

The Issue: The firm has become aware of the potential for disruption (flickering) in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 29, 2016· Corin USA Limited

Recalled Item: Trinity Acetabular Shell Product Usage: Total Hip Replacement. Recalled by...

The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: software for Syngo Dynamics a Picture Archiving and Communication System...

The Issue: Siemens is releasing a software update that addresses an issue of mixing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Biomet, Inc.

Recalled Item: Crosslock DVR ePAK -Sterile Recalled by Biomet, Inc. Due to Foreign Object...

The Issue: Components of the DVR ePAKs can oxidize during shipment and storage prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Novadaq Technologies Inc.

Recalled Item: PINPOINT Endoscopic Fluorescence Imaging System Recalled by Novadaq...

The Issue: It has been determined that the PINPOINT Operator's Manual does not contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Corin USA Limited

Recalled Item: Trinity Acetabular Shell Product Usage Total Hip Replacement. Recalled by...

The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Valeant Pharmacueticals International

Recalled Item: Orapharma (Onpharma) Onset Mixing Pen Rx only Recalled by Valeant...

The Issue: It has been determined that the Onset Mixing Pen has an optimal use period...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2016· Physio-Control, Inc.

Recalled Item: LIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature...

The Issue: The firm became aware that when using EtC02 in the kPa or % setting and in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FMC7 FITC: Model 430918. FMC7 is intended for in Recalled by Becton,...

The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 25, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS)...

The Issue: Siemens' conducting a recall due to a potential issue when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PRECSION PRM 18FR SIL FLY Item Code: PP18SD Recalled by...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover P400 PREM U/M 18FR SIL COUDE CATH SECURE Recalled by Covidien...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PPREM 18FR UL LTX FOLEY TRY CSD Item Recalled by Covidien LLC...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover P400 PREM U/M 16FR SLVR FLY Item Code: Recalled by Covidien...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover P400 PREM U/M 16FR UL FOLY CSD Item Recalled by Covidien LLC...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover 400 PREM U/M 18FR SLVR FLY Item Code: Recalled by Covidien...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PREM U/M 14FR TMP SNS CSD Item Code: Recalled by Covidien LLC...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover P400 UM 16FR SIL COUDE SECURE Item Code: Recalled by Covidien...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover MIDSTREAM KIT CASTILE SOAP Item Code: 2090SA Castile Recalled...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing