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 4586145880 of 46,762 recalls

DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: DMSO / BUPIVACAINE HCL 50%/0.5% INJECTABLE 100 ML Recalled by Franck's Lab...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: CHORIONIC GONADOTROPIN (STANDARD) - 21 DAY 200 UNIT VIALS KIT 1 KIT Recalled...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: ACETAZOLAMIDE Recalled by Franck's Lab Inc., d.b.a. Franck's Compounding Lab...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Franck's Lab Inc., d.b.a. Franck's Compounding Lab

Recalled Item: FOLIC ACID 10MG/ML INJECTABLE 60 ML (1 PRODUCT) Recalled by Franck's Lab...

The Issue: Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Mallinckrodt Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...

The Issue: CGMP Deviations: This product is being recalled because expired flavoring...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2012· Mallinckrodt Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution Recalled by...

The Issue: Subpotent (Multiple Ingredient) Drug: Low out of specification assay results...

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

Class III — Low RiskOngoing
Refund
FoodMay 25, 2012· Hocean Inc

Recalled Item: Nitre powder. Brand "Selected Product" Recalled by Hocean Inc Due to FDA...

The Issue: FDA analysis of the product found that the product consisted of mainly...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 25, 2012· Bumble Bee International

Recalled Item: Bumble Bee Fancy Whole Oysters 12/8 oz can. Recalled by Bumble Bee...

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
Medical DeviceMay 25, 2012· CareFusion 303, Inc.

Recalled Item: Alaris PC unit model 8015 Product Usage: The device is Recalled by...

The Issue: The recall was initiated because the Alaris PC unit model 8015 has a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 24, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of inaccurate Scale factor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2012· GE Healthcare, LLC

Recalled Item: GE Seno Advantage 1.x Recalled by GE Healthcare, LLC Due to GE Healthcare...

The Issue: GE Healthcare has become aware of an issue associated with the magnification...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Advantage Workstations Recalled by GE Healthcare, LLC Due to...

The Issue: GE Healthcare is informing you of incorrect measurements when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2012· GE Healthcare, LLC

Recalled Item: GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume...

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

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

Class II — Potential Health HazardOngoing
FoodMay 23, 2012· Mitsui Foods Inc

Recalled Item: Whole Oysters: 1) Empress Whole Oysters Recalled by Mitsui Foods Inc Due to...

The Issue: As of May 1, Korean shellfish imports have been blocked by the United States...

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

Class III — Low RiskOngoing
Refund
FoodMay 23, 2012· Mitsui Foods Inc

Recalled Item: Smoked Oysters: 1) Empress Smoked Oysters In Cottonseed Oil Recalled by...

The Issue: As of May 1, Korean shellfish imports have been blocked by the United States...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 23, 2012· LMA North America Inc

Recalled Item: LMA Esophageal Intubation Detector (EID) Recalled by LMA North America Inc...

The Issue: The recall was initiated because LMANA has received a complaint that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2012· Integra Limited

Recalled Item: Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R)...

The Issue: The Integra(TM) Jarit(R) Take-Apart Laparoscopic Instrument shafts were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2012· Stingray Surgical Products, LLC

Recalled Item: Bipolar Forceps model number: S02-XXX Recalled by Stingray Surgical...

The Issue: On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: IntelliSpace Portal software and Extended Brillance Workspace software...

The Issue: The Intellispace Portal software and Extended Brillance Workspace software...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal software. Intellispace Portal is a multimodality thin...

The Issue: Philips is issuing a software update to the Intellispace Portal systems to...

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

Class II — Potential Health HazardOngoing