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. 2,283 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,283 in last 12 months

Showing 4228142300 of 46,762 recalls

FoodJune 28, 2013· Priester Pecan Company, Inc.

Recalled Item: PRIESTER'S PECANS brand NUTTY FAVORITES ASST Recalled by Priester Pecan...

The Issue: Pistachios, which were supplied by ARO and subsequently recalled, have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's OsteoSheath 4 Enhanced Bone Support Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Osteosheath 4...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's Fem-Vite Women's Anti-Oxidant Formula Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Fem-Vite was...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 28, 2013· Vinco Inc.

Recalled Item: Vinco's OsteoSheath Enhanced Bone Support Recalled by Vinco Inc. Due to...

The Issue: The soy ingredient used to manufacture certain lots of Vinco's Osteosheath...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 28, 2013· Alphatec Spine, Inc.

Recalled Item: Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico Recalled by...

The Issue: The firm initiated this recall of certain lots of Illico Ti Cannulated...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Calibrator A. Cat. #04800735 Recalled by Siemens Healthcare...

The Issue: Calibrator A lot CA77 is under-recovering to the assigned target for the...

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

Class III — Low RiskOngoing
Medical DeviceJune 28, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...

The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal Reverse Shoulder System Instrumentation Recalled by Zimmer,...

The Issue: There is potential for one or both tabsof theTrabecular Metal Reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2013· Medtronic Neurosurgery

Recalled Item: Medtronic Preimplantation Test Kit Recalled by Medtronic Neurosurgery Due to...

The Issue: Medtronic Neurosurgery is recalling the Medtronic Preimplantation Test Kit...

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

Class II — Potential Health HazardOngoing
DrugJune 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Silver Sword capsules Recalled by Fabscout Entertainment, Inc Due to...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2013· Fabscout Entertainment, Inc

Recalled Item: Clalis capsules Recalled by Fabscout Entertainment, Inc Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Hospira Inc.

Recalled Item: Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer report of visible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent Drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2013· Max Huber Research Labs, Inc.

Recalled Item: LA MER the spf 18 fluid tint Recalled by Max Huber Research Labs, Inc. Due...

The Issue: Subpotent drug: Avobenzone 3%, one of the active sunscreen ingredients may...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 27, 2013· Insight Instruments, Inc.

Recalled Item: MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25-...

The Issue: The product was registered and distributed as a Class I medical device and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Mar Cor Purification

Recalled Item: Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model...

The Issue: High inlet water pressure beyond specification and the solenoid valve does...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: ADVIA 120 Hematology Analyzer Recalled by Siemens Healthcare Diagnostics Due...

The Issue: The ADVIA 120 optics cover or hood is located on the very top of the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers Recalled...

The Issue: Customers complained of a positive bias in patient results on the IMMULITE/...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS zee and zeego x-ray Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens issued a customer safety advisory notice and field safety corrective...

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

Class II — Potential Health HazardOngoing