Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,348 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,348 in last 12 months

Showing 2384123860 of 27,254 recalls

Medical DeviceJanuary 8, 2014· B. Braun Medical, Inc.

Recalled Item: SAFSITE¿ Injection Sites and IV Sets manufactured with SAFSITE¿ Injection...

The Issue: Complaints were received reporting leakage on certain lots of SAFSITE¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panaroma Central Station Product Usage: This device can view real time...

The Issue: Mindray has identified two issues with the Panorama Central Station. Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· The Anspach Effort, Inc.

Recalled Item: ANSPACH Cutting bur Recalled by The Anspach Effort, Inc. Due to Anspach...

The Issue: Anspach product code L-3SD contained product code S-3SD which is shorter in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2014· Churchill Medical Systems, Inc.

Recalled Item: AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular...

The Issue: Defective component may cause extension sets to leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2014· Synthes, Inc.

Recalled Item: Drill Template and the Saw Guide for the Ulna Osteotomy Recalled by Synthes,...

The Issue: The Drill Template and the Saw Guide for the Ulna Osteotomy System may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2014· Synthes, Inc.

Recalled Item: Synthes Driving Cap/Threaded Both parts are intended for use in Recalled by...

The Issue: The Synthes Driving Cap/Threaded can bind in the IM Nail Radiolucent...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ PCR Urine Kit 100 PKT IVD cobas¿ PCR Female Recalled by Roche...

The Issue: Numerous complaints have been filed that leaking cobas ¿ PCR media 4.3 mL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Boston Scientific Corporation

Recalled Item: Atlantis PV Recalled by Boston Scientific Corporation Due to Reports of...

The Issue: Reports of physicians experiencing inability to pass a 0.035" guidewire...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Enzyme 1 Calibrator (ENZ 1 CAL) lots 3FD034 Recalled by...

The Issue: Complaints were received regarding Quality Control (QC) shifts with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Zimmer Dental Inc

Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...

The Issue: Zimmer Dental is conducting a voluntary recall of a single lot of the...

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

Class II — Potential Health HazardOngoing