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 4124141260 of 46,762 recalls

Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS brand ARTISTE Linear Accelerator Linac systems with component: any...

The Issue: A safety risk regarding a potentially existing dark current radiation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS brand ONCOR series Linear Accelerator Linac systems with component:...

The Issue: A safety risk regarding a potentially existing dark current radiation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Alere San Diego, Inc.

Recalled Item: Product Brand Name(s): Alere Cholestech LDX¿ Lipid Profile"GLU Test Cassette...

The Issue: Alere initiated a recall of Cholestech LDX Lipid Profile-GLU test cassettes,...

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

Class III — Low RiskOngoing
Medical DeviceOctober 23, 2013· ConMed Corporation

Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...

The Issue: The affected lots were exposed to a higher than acceptable level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster 500 Recalled by Carl Zeiss Meditec, Inc. Due to The...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster Recalled by Carl Zeiss Meditec, Inc. Due to The user...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· ConMed Corporation

Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...

The Issue: The affected lots were exposed to a higher than acceptable level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable Recalled by...

The Issue: It was reported that the siderail may appear latched when it is not, due to...

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

Class II — Potential Health HazardOngoing
DrugOctober 22, 2013· Sandoz Incorporated

Recalled Item: Tacrolimus Capsules Recalled by Sandoz Incorporated Due to Cross...

The Issue: Cross Contamination with Other Products: findings of carryover of trace...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2013· Medisca Inc.

Recalled Item: Human Chorionic Gonadotropin Recalled by Medisca Inc. Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; Firm states that erroneous...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: SuperDigestZyme (Z22) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: RepairVite (K63) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: GlutenFlam (K-52) Enzyme & Bioflavonoid Dietary Supplement Recalled by Apex...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2013· Apex Energetics

Recalled Item: LGS-Zyme (Z12) Recalled by Apex Energetics Due to Apex Energetics is...

The Issue: Apex Energetics is recalling GlutenFlam, SuperDigestZyme, LGS-Zyme, and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ProVia¿ CROSSING GUIDEWIRE Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing