Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,423 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,423 in last 12 months

Showing 2174121760 of 27,833 recalls

Medical DeviceMay 21, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Healthcare Diagnostics Dimension Vista Systems Recalled by Siemens...

The Issue: Two software issues may occur in Vista software version 3.6.1. Issue #1:...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2015· Exactech, Inc.

Recalled Item: Exactech Single Barrel Drill Guides The Single Barrel Drill Guide Recalled...

The Issue: Shipped to a single consignee prior to completion of final inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Bicarbonate Concentrate (Dialysate Concentrate for...

The Issue: Bacterial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2015· Northern Digital Inc.

Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...

The Issue: Inadequate curing of adhesive, which may cause the two halves of the spheres...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: CentraLink" Data Management System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has determined that the sample query function...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Remel Inc

Recalled Item: VersaTREK Instrument Series 240 Recalled by Remel Inc Due to Use of the...

The Issue: Use of the recalled product may result in false positive reports.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Tni-Ultra Assay Recalled by Siemens Healthcare Diagnostics,...

The Issue: System-to-system bias between the Tni-Ultra assay on the ADVIA Centaur CP...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Remel Inc

Recalled Item: VersaTREK Instrument Series 528 Recalled by Remel Inc Due to Use of the...

The Issue: Use of the recalled product may result in false positive reports.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2015· Pointe Scientific, Inc.

Recalled Item: Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml Recalled by...

The Issue: A reduction in the reconstituted stability has been identified. Clinicians...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2015· Zimmer, Inc.

Recalled Item: M/L Taper with Kinectiv¿ Technology. prosthesis Recalled by Zimmer, Inc. Due...

The Issue: Zimmer is initiating a voluntary recall of 64 lots (752 implants total) of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 18, 2015· Edwards Lifesciences, LLC

Recalled Item: ClearSight Recalled by Edwards Lifesciences, LLC Due to Edward Lifesciences...

The Issue: Edward Lifesciences is recalling the ClearSight System because the finger...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· ArthroCare Medical Corporation

Recalled Item: PROcise XP Wand with Integrated Cable Product Usage: Recalled by ArthroCare...

The Issue: Potential component failure resulting in inoperability

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· MedtestDx, Inc.

Recalled Item: MedTest DX Control Reconstitution Fluid Kit configuration: 20 x 5 Recalled...

The Issue: Vial to vial variation in the fill volume that could affect control recovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· ArthroCare Medical Corporation

Recalled Item: EVAC 70 XTRA with Integrated Cable Product Usage: Recalled by ArthroCare...

The Issue: Potential component failure causing device inoperability

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via and Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: measurements drawn on the 2nd and subsequent images of the series are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· Veridex, LLC

Recalled Item: Cell Search Circulating Tumor Kit. Intended for the enumeration of Recalled...

The Issue: Complaints of the presence of artifacts that appears as small bead like...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2015· Philips Ultrasound, Inc.

Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound, Inc. Due to Philips...

The Issue: Philips Healthcare has discovered a problem in the Philips Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2015· Cook Inc.

Recalled Item: LapSac Surgical Tissue Pouch. The current intended use for the Recalled by...

The Issue: Includes Information not stated in the intended use.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2015· BIOMET FRANCE S.A.R.L.

Recalled Item: The Optigun Ratchet is a hand-held cement gun for use Recalled by BIOMET...

The Issue: The pin which maintains the knob button, may disconnect and become lost....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2015· Teleflex Medical

Recalled Item: Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson...

The Issue: The intake port may be blocked which can cause the bag to fail to fill.

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

Class I — Serious Health HazardOngoing