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 4036140380 of 46,762 recalls

Medical DeviceFebruary 17, 2014· Elekta, Inc.

Recalled Item: XiO RPT System The XiO RTP System is used to Recalled by Elekta, Inc. Due to...

The Issue: Dose and Monitor Unit values are not computed correctly when Elekta...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart XL Recalled by Philips Medical Systems, Inc. Due to...

The Issue: Philips HeartStart XL may experience a power board failure causing failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2014· RAYSEARCH LABORATORIES AB

Recalled Item: RaySearch Ray Station Radiation Therapy Treatment Planning System Recalled...

The Issue: RaySearch Laboratories has recalled "RaySearch Ray Station 2.0, 2.5, 3.0,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima CT580/Discovery CT590RT scanners running software...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2014· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s):...

The Issue: HORIBA Medical initiated this recall of all software versions of ABX PENTRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2014· Spacelabs Healthcare, Llc

Recalled Item: Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11...

The Issue: Spacelabs has voluntarily recalled G2 Clinical Access Software CD because...

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

Class II — Potential Health HazardOngoing
DrugFebruary 14, 2014· Ben Venue Laboratories Inc

Recalled Item: Acetylcysteine Solution Recalled by Ben Venue Laboratories Inc Due to...

The Issue: Presence of Particulate Matter: During a review of retain samples, the firm...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 14, 2014· Agila Specialties Private Ltd.

Recalled Item: etomidate injection Recalled by Agila Specialties Private Ltd. Due to...

The Issue: Presence of Particulate Matter: Potential for small black particles to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 14, 2014· Legacy Pharmaceutical Packaging

Recalled Item: Fluoxetine Capsules Recalled by Legacy Pharmaceutical Packaging Due to...

The Issue: Chemical Contamination: The recalling firm received notice that their...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 14, 2014· Medisca Inc

Recalled Item: CITRULLINE (L) in 25 g Recalled by Medisca Inc Due to Labeling: Label...

The Issue: Labeling: Label Mix-Up: FDA tested samples of API from Medisca, labeled as...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 13, 2014· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2014· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 13, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version...

The Issue: GE Healthcare has recently become aware of a potential safety issue with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: MULTIX FUSION. The Multix Fusion system is a radiographic system Recalled by...

The Issue: It was observed that the corrugated hose holder above the 3D rail on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2014· Accumetrics Inc

Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...

The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa test because it may result...

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

Class II — Potential Health HazardOngoing
FoodFebruary 13, 2014· Northern Valley Baking Co.

Recalled Item: The Other Macaroon G'nache P'nache 5.3 oz. Manufactured and Distributed...

The Issue: Northern Valley Baking Company did not declare milk or soy on the allergen...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2014· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2014· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 12, 2014· Abbott Laboratories

Recalled Item: ARCHITECT Intact PTH Controls consists of 3 x 1 Bottle Recalled by Abbott...

The Issue: Abbott has confirmed that a performance shift in the ARCHITECT Intact PTH...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2014· Abbott Laboratories

Recalled Item: ARCHITECT Intact PTH Calibrators consists of 6 bottles (4.0 mL Recalled by...

The Issue: Abbott has confirmed that a performance shift in the ARCHITECT Intact PTH...

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

Class II — Potential Health HazardOngoing