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. 2,245 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,245 in last 12 months

Showing 4574145760 of 46,762 recalls

Medical DeviceMay 30, 2012· SALTER LABS

Recalled Item: Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7...

The Issue: A complaint was received, and later verified, that product labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2012· Abbott Laboratories

Recalled Item: ARCHITECT CA 19-9XR Reagent Kit Recalled by Abbott Laboratories Due to The...

The Issue: The six ARCHITECT CA 19-9XR reagent lots are demonstrating a shift up in...

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

Class II — Potential Health HazardOngoing
FoodMay 29, 2012· Aldi Inc

Recalled Item: Northern Catch Harvest of the Sea Fancy Whole Oysters and Recalled by Aldi...

The Issue: The product has been prepared, packed, or held under insanitary conditions...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 29, 2012· Camerican International

Recalled Item: Whole Oysters in Water under the following brand names: 1) Recalled by...

The Issue: Inspectional evidence and sample analyses as well as reports of food borne...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 29, 2012· Camerican International

Recalled Item: Smoked Oysters In cottonseed oil sold under the following brand Recalled by...

The Issue: Inspectional evidence and sample analyses as well as reports of food borne...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 29, 2012· World Finer Foods, Inc.

Recalled Item: Reese Petite Smoked Oysters. Distributed by: World Finer Foods Recalled by...

The Issue: According to information published by the FDA: Because of inadequate...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 29, 2012· World Finer Foods, Inc.

Recalled Item: Reese Colossal Smoked Oysters. Distributed by: World Finer Foods Recalled by...

The Issue: According to information published by the FDA: Because of inadequate...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 29, 2012· Camerican International

Recalled Item: Northern Catch Fancy Whole Oysters Net Wt. 8 OZ (227g) Recalled by Camerican...

The Issue: Inspectional evidence and sample analyses as well as reports of food borne...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodMay 29, 2012· World Finer Foods, Inc.

Recalled Item: Reese Medium Smoked Oysters. Distributed by: World Finer Foods Recalled by...

The Issue: According to information published by the FDA: Because of inadequate...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 29, 2012· IDEV Technologies, Inc.

Recalled Item: IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent...

The Issue: There was an error on the outer labeling of this device. The inner label was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...

The Issue: The Positive Control for the Captia Varicella-Zoster Virus (VZV) IgG Kit has...

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

Class III — Low RiskOngoing
Medical DeviceMay 29, 2012· Alcon Research, LTD.

Recalled Item: This voluntary medical device correction is related to Alcon products...

The Issue: This medical device correction is related to Alcon products that present a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo(R) Lab Data Manager and syngo(R) Lab Process Manager Recalled by...

The Issue: When using the syngo Quality Control package the system may not perform as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Alphatec Spine, Inc.

Recalled Item: TRESTLE LUXE¿ Anterior Cervical Plating System Recalled by Alphatec Spine,...

The Issue: On May 9th 2012 Alphatec Spine received a complaint which reported that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: EasyLink Informatic System is included with the Dimension Vista System....

The Issue: When using the EasyLink Quality Control Package the system may not perform...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Mckesson Medical Imaging Group

Recalled Item: Horizon Medical Imaging system. Product Usage: Horizon Medical Imaging is...

The Issue: There is a potential to save reports in RadReport with an Incorrect Final...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Carefusion 2200 Inc

Recalled Item: AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector...

The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2012· Carefusion 2200 Inc

Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...

The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2012· Carefusion 2200 Inc

Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...

The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2012· Microbiologics Inc

Recalled Item: Microbiologics 217 Osseo Avenue North Recalled by Microbiologics Inc Due to...

The Issue: Microbiologics is recalling a number of lots of KWIK-QC Gram Stain Slides....

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

Class II — Potential Health HazardOngoing