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. 2,361 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,361 in last 12 months

Showing 2196121980 of 27,254 recalls

Medical DeviceJanuary 14, 2015· INO Therapeutics (dba Ikaria)

Recalled Item: Ikaria Recalled by INO Therapeutics (dba Ikaria) Due to Potential delivery...

The Issue: Potential delivery failure alarm condition. INOmax DSIR with software...

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

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

Recalled Item: AQUAPAK 101 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: ADAPTOR Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: Hudson RCI¿ Humidifier Adaptor Recalled by Teleflex Medical Due to Foreign...

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUA 540 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

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

Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination

The Issue: The packages may contain foreign material (black particles).

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· Teleflex Medical

Recalled Item: LMA (Laryngeal Mask Airway) Supreme (New Cuff) Size 5 Recalled by Teleflex...

The Issue: The labelling of units from the affected lot indicates that it contains a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· CareFusion 303, Inc.

Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion set due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza: Syngo.plaza is a Picture Archiving and Communication System...

The Issue: In case of a system crash, images may not be written to the hard disk and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2015· Medtronic Sofamor Danek USA Inc

Recalled Item: KYPHON EXPRESS Recalled by Medtronic Sofamor Danek USA Inc Due to The...

The Issue: The product, labeled as containing, one bevel-tipped instrument and one...

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

Class II — Potential Health HazardOngoing