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 4378143800 of 46,762 recalls

Medical DeviceMarch 20, 2013· Biomet U.K., Ltd.

Recalled Item: Oxford Uni Knee System Recalled by Biomet U.K., Ltd. Due to Investigation of...

The Issue: Investigation of complaints found excessive use of the instrument could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: HORIBA ABX PENTRA 400 I.S.E. Module Recalled by Horiba Instruments, Inc dba...

The Issue: HORIBA Medical is informing all ABX PENTRA 400 Analyzer with I.S.E. Module...

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

Class II — Potential Health HazardOngoing
DrugMarch 19, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Disulfiram Tablets USP 250 mg Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: CGMP Deviation; cotton coil is missing in some packaged bottles

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

Class III — Low RiskOngoing
Refund
DrugMarch 19, 2013· Dr. Reddy'S Laboratories

Recalled Item: Tizanidine Tablets USP Recalled by Dr. Reddy'S Laboratories Due to Labeling...

The Issue: Labeling Illegible: There is a possibility that the bottle labels do not...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 19, 2013· Hospira Inc.

Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...

The Issue: Some patients are obtaining access to the dosage reset codes required to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2013· Hospira Inc.

Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...

The Issue: Some patients are obtaining access to the dosage reset codes required to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2013· Accuray Incorporated

Recalled Item: Accuray CyberKnife System Medical Physicist Recalled by Accuray Incorporated...

The Issue: A defect on the master-side connector block of the pneumatic tool changer...

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2013· Boehringer Ingelheim Roxane Inc

Recalled Item: Oxcarbazepine Tablets Recalled by Boehringer Ingelheim Roxane Inc Due to...

The Issue: SubPotent Drug: The firm discovered out of specification results for assay...

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

Class III — Low RiskOngoing
Refund
DrugMarch 18, 2013· Apotex Corp.

Recalled Item: Piperacillin and Tazobactam for Injection Recalled by Apotex Corp. Due to...

The Issue: Crystallization: Potential to exhibit precipitation/crystallization in IV...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 18, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Donnatal Extentabs Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Bottled product is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2013· Reckitt Benckiser Inc

Recalled Item: Cherry Cepacol Sore Throat Lozenges Recalled by Reckitt Benckiser Inc Due to...

The Issue: Subpotent Drug: Product did not conform to the 18-month stability test...

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

Class III — Low RiskOngoing
Refund
DrugMarch 18, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Ethambutol Hydrochloride Tablets Recalled by West-ward Pharmaceutical Corp....

The Issue: Subpotent Drug: Out Of Specification results for assay at the stability...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 18, 2013· Magno Humphries Inc

Recalled Item: Ferrous Sulfate Tablets 325 mg Recalled by Magno Humphries Inc Due to The...

The Issue: The firm found minute pieces of blue material identified by their raw...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: PSS Select medical products***Biopsy Punches*** Disposable manual instrument...

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy....

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Shimadzu Medical Systems

Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...

The Issue: The recall was initiated because Shimadzu Corporation has identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: HD Still Capture System ConMed Linvatec . Captures Recalled by Linvatec...

The Issue: The VP1600 HD Still Capture Image System is recalled due to an anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...

The Issue: Devices were not sealed correctly during the manufacturing process, and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...

The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...

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

Class I — Serious Health HazardOngoing