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. 2,258 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,258 in last 12 months

Showing 4384143860 of 46,762 recalls

DrugMarch 12, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Portia (levonorgestrel and ethinyl estradiol) Tablets Recalled by Teva...

The Issue: Failed Tablet/Capsule Specifications: This recall is being carried out due...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 12, 2013· Custom Ultrasonics, Inc.

Recalled Item: Custom Ultrasonics System 83 Plus 2 and Plus 9 Endoscope Washer/Disinfector....

The Issue: Certain System 83 Plus 2 and System 83 Plus 9 units running the Windows 7...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· GE Healthcare It

Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Berchtold Corp.

Recalled Item: Hand Controls for Operon D750 Recalled by Berchtold Corp. Due to The firm...

The Issue: The firm received complaints for unintended movements.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 16-Slice Water Recalled by Philips Medical Systems (Cleveland)...

The Issue: Philips Healthcare received a report from the field stating when they viewed...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2013· Green Planet Inc

Recalled Item: Night Bullet Capsules Recalled by Green Planet Inc Due to Marketed Without...

The Issue: Marketed Without an Approved NDA/ANDA; product contains analogues of...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 11, 2013· Hi-Tech Pharmacal Co., Inc.

Recalled Item: Acetic Acid Otic Solution Recalled by Hi-Tech Pharmacal Co., Inc. Due to...

The Issue: Subpotent Drug: The product/lot is out-of-specification (OOS) for the assay...

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

Class III — Low RiskOngoing
Refund
DrugMarch 11, 2013· Gsms

Recalled Item: LISINOPRIL AND HYDROCHLOROTHIAZIDE TABLETS Recalled by Gsms Due to Presence...

The Issue: Presence of Foreign Substance: Reports of gray smudges identified as minute...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 11, 2013· Nashua Nutrition

Recalled Item: Proti Diet High Protein Chocolate Dream Bar Recalled by Nashua Nutrition Due...

The Issue: Product may be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 11, 2013· GE Healthcare It

Recalled Item: Centricity Perinatal and Centricity Intensive Care is intended to be...

The Issue: 1) Under rare network conditions, a Centricity Perinatal process may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2013· Becton Dickinson & Co.

Recalled Item: BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood. Used Recalled by...

The Issue: Microbiological media may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2013· Becton Dickinson & Co.

Recalled Item: BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood and Recalled by Becton...

The Issue: Microbiological media may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2013· Becton Dickinson & Co.

Recalled Item: BBL(tm) CDC Anaerobe 5% Sheep Blood Agar. Used for culturing microorganisms....

The Issue: Microbiological media may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2013· Lifescan Inc

Recalled Item: All OneTouch Verio IQ Blood Glucose Meters sold as: Verio Recalled by...

The Issue: The Verio IQ meter will shut off and revert to set up mode at glucose values...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 11, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dade(R) Actin(R) FSL Activated PTT Reagent. For use in the Recalled by...

The Issue: Siemens has observed that the listed lot numbers show an increase in Heparin...

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

Class II — Potential Health HazardOngoing
FoodMarch 9, 2013· La Preferida Inc

Recalled Item: Metal cans Recalled by La Preferida Inc Due to Some cans may not have been...

The Issue: Some cans may not have been fully processed which could result in product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: LifeCare PCA Infusion System with Hospira MedNet Software Recalled by...

The Issue: Screw rotation error occurring when the pump detects a mismatch between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: LifeCare PCA 3 Recalled by Hospira Inc. Due to Screw rotation error...

The Issue: Screw rotation error occurring when the pump detects a mismatch between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: The LifeCare PCA Plus II infusion pump system is designed for safe Recalled...

The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2013· Hospira Inc.

Recalled Item: The PCA 3 system cam be used in a wide range of clinical settings Recalled...

The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...

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

Class II — Potential Health HazardOngoing