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. 2,353 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,353 in last 12 months

Showing 2256122580 of 27,254 recalls

Medical DeviceOctober 6, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur BNP Assay for in vitro diagnostic use in Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed that approximately 2000...

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

Class III — Low RiskOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips Avalon Monitors with software revision J.30.58: Model Product FM20...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips IntelliVue Monitors with software revisions J.21.03 Recalled by...

The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2014· Zimmer, Inc.

Recalled Item: Natural Knee II Revision Femoral Stem Recalled by Zimmer, Inc. Due to Failed...

The Issue: Failed to meet established requirements for sterile barrier integrity due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...

The Issue: Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer Dental Inc

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

The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Roscoe Medical Inc

Recalled Item: Transport Rollator with Padded Seat Recalled by Roscoe Medical Inc Due to...

The Issue: The caster may separate completely from the device frame causing injury to user.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer, Inc.

Recalled Item: Continuum Acetabular System Trabecular Metal Shell with Multi Holes Recalled...

The Issue: The affected products are missing polar boss threads.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Zimmer Dental Inc

Recalled Item: Spline Twist Implant Recalled by Zimmer Dental Inc Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2014· Medartis, Inc.

Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...

The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2014· Masimo Corporation

Recalled Item: Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Recalled by...

The Issue: Firm has identified a small number of Oximetry Cables with crossed-internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension HB1C Flex reagent cartridge Recalled by Siemens Healthcare...

The Issue: Certain lots of the reagent cartridges show confirmed positive bias...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2014· Signal Medical Corporation

Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...

The Issue: Packaging of a device was compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Coloplast Manufacturing US, LLC

Recalled Item: Coloplast Conveen Urine Collection Leg Bag Recalled by Coloplast...

The Issue: Coloplast is recalling the Conveen Contour Leg Bag due to potential leakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Smiths Medical ASD, Inc.

Recalled Item: CADD-Solis Medication Safety Software Recalled by Smiths Medical ASD, Inc....

The Issue: Smiths Medical has identified an issue with a single batch (Lot Number...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Merge Healthcare, Inc.

Recalled Item: Merge Healthcare Recalled by Merge Healthcare, Inc. Due to It has been...

The Issue: It has been reported that during use, the SpO2 value displayed on the Hemo...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2014· Integra LifeSciences Corp.

Recalled Item: Integra Selector Kit Sterile single use device A bi-lumen Recalled by...

The Issue: Some specific lots of Selector Tubing may potentially leak irrigation fluid...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Biomet, Inc.

Recalled Item: Mamba Disposable Nitinol Needle. The Biomet Sports Medicine Mamba...

The Issue: An investigation identified that high level friction may exist between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Amerx Health Care Corp.

Recalled Item: Amerigel Saturated Gauze Dressing Wound management Recalled by Amerx Health...

The Issue: Formulation deviation

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Calibrator E Recalled by Siemens Healthcare Diagnostics, Inc Due to...

The Issue: Positive bias for Calibrator E lot kits ending in 38 and 39 with the ADVIA...

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

Class II — Potential Health HazardOngoing