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. 2,299 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,299 in last 12 months

Showing 3918139200 of 46,762 recalls

FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: Market Pantry Apple Cinnamon Recalled by PUREFRUIT CHILE S.A Due to...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: fruty U applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: fruty U applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 1, 2014· Ansar Group, Inc. Dba Ansar Medical Technologies, Inc

Recalled Item: Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor Recalled...

The Issue: The blood pressure (BP) circuit occasionally fails to inflate the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· PerkinElmer Health Sciences, Inc.

Recalled Item: Panthera-Puncher 9 . Panthera-Puncher 9 is a sample transfer instrument...

The Issue: Risk of incorrect results from samples prepared with Panthera-Puncher 9

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

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

Recalled Item: Moore Hip Prosthesis Long Fenestrated Stem 38 mm (1-1/2 Inch) Recalled by...

The Issue: Zimmer is initiating a voluntary recall of 20 production lots of Moore Hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Ra Medical Systems Inc

Recalled Item: PHAROS Excimer Laser Recalled by Ra Medical Systems Inc Due to RA Medical...

The Issue: RA Medical Systems is recalling the PHAROS EX-308 Excimer Laser because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Steris Corporation

Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The...

The Issue: STERIS has identified that deformation of the washers door handle pin may...

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

Class III — Low RiskOngoing
Medical DeviceJune 30, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo Imaging XS Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens has become aware of the potential malfunction when using syngo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Invivo Corporation

Recalled Item: Philips IP5 Information Portal The Expression Information Portal (Model IP5)...

The Issue: The wireless function of the IP5 radio could be interrupted causing loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Teleflex Medical

Recalled Item: RUSCH Recalled by Teleflex Medical Due to There is a possibility the handle...

The Issue: There is a possibility the handle of the laryngoscope may heat up and melt...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2014· Brainlab AG

Recalled Item: Patient Data Manager 2.0 (Content manager 2.0 Recalled by Brainlab AG Due to...

The Issue: The following defects have been identified for data loaded with Patient Data...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2014· Steris Corporation

Recalled Item: The STERIS 4085 General Surgical Table Product Usage: is an Recalled by...

The Issue: STERIS engineering analysis has determined the D1 pressure switch in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2014· Life Force of Tampa, LLC

Recalled Item: Life Force Chamber Product Usage:The product is intended for restful...

The Issue: The Life Force chamber is marketed and promoted as a medical device,...

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

Class II — Potential Health HazardOngoing
DrugJune 27, 2014· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2014· Poly Pharmaceuticals, Inc

Recalled Item: LORTUSS EX Recalled by Poly Pharmaceuticals, Inc Due to Does Not Meet...

The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 26, 2014· Poly Pharmaceuticals, Inc

Recalled Item: POLY-TUSSIN AC LIQUID Recalled by Poly Pharmaceuticals, Inc Due to Does Not...

The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 26, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...

The Issue: CGMP Deviations: These products are being recalled because they were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...

The Issue: CGMP Deviations: These products are being recalled because they were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 26, 2014· Alphatec Spine, Inc.

Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...

The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...

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

Class II — Potential Health HazardOngoing