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 3984139860 of 46,762 recalls

DrugApril 29, 2014· Independent Nutrition Center, Inc.

Recalled Item: Red Yeast Rice High Potency Dietary Supplement Recalled by Independent...

The Issue: Marketed Without An Approved NDA/ANDA: Product is being recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable...

The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Sterile Water for Injection Recalled by Flawless Beauty LLC Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection...

The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Vitamin C (ascorbic acid) Injection Recalled by Flawless Beauty LLC Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2014· Flawless Beauty LLC

Recalled Item: Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution...

The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 28, 2014· Baxter Healthcare Corporation

Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...

The Issue: Connection issues between the PD transfer set catheter connector and an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2014· Atrium Medical Corporation

Recalled Item: Atrium Express Dry Seal Chest Drain ATS Blood Recovery Recalled by Atrium...

The Issue: Product that was previously recalled because the Chest Drain tubing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2014· Greatbatch Medical

Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...

The Issue: Greatbatch identified that the documentation does not support the five-year...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· CryoLife, Inc.

Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...

The Issue: Serum albumin component monomer failed to meet internally established end of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...

The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2014· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...

The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...

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

Class II — Potential Health HazardOngoing
DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

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

Class III — Low RiskOngoing
Refund
DrugApril 25, 2014· Prestige Brands Holdings

Recalled Item: PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold Recalled by Prestige Brands...

The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 25, 2014· Hitachi Medical Systems America Inc

Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...

The Issue: The firm received a complaint stating the Coil Extension Cable accessory...

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

Class II — Potential Health HazardOngoing
FoodApril 25, 2014· Kroger Co

Recalled Item: Private Selection Caramel Hazelnut Fudge Truffle Ice Cream Recalled by...

The Issue: The firm discovered that the label for two of their products did not declare...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 25, 2014· Kroger Co

Recalled Item: Private Selection Chocolate Hazelnut Mascarpone Ice Cream Recalled by Kroger...

The Issue: The firm discovered that the label for two of their products did not declare...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Composix" LIP Mesh with Echo PS" 8"x10" Reorder Number: Recalled by...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Composix" LP with Echo PS" 6x10 Reorder Number: 0144610 Indicated Recalled...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

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

Class II — Potential Health HazardOngoing