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. 2,251 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,251 in last 12 months

Showing 4430144320 of 46,762 recalls

Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 1 inch Coated Needle with Extended...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: Electrosurgical Tip Cleaner Recalled by ConMed Corporation Due to ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade Recalled...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - SHARP Recalled by ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: TUR/Endoscopic Cable Recalled by ConMed Corporation Due to ConMed received...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: CONMED(R) ELECTROSURGICAL SAFETY HOLSTER Recalled by ConMed Corporation Due...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2012· ConMed Corporation

Recalled Item: UltraClean(R) Accessory Electrode 6 inch Coated Blade Recalled by ConMed...

The Issue: ConMed received complaints of some devices which had broken through the seal...

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2012· D& S Herbals, LLC

Recalled Item: Super Power capsules Recalled by D& S Herbals, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA: This dietary supplement has been...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2012· Lee Pharmaceuticals, Inc

Recalled Item: 12-Hour Sinus (oxymetazoline hydrochloride) Nasal Spray Recalled by Lee...

The Issue: Microbial Contamination of a Non-Sterile Products: 12-Hour Sinus Nasal Spray...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2012· Warner Chilcott Company LLC

Recalled Item: Femtrace 0.45 mg (Estradiol Acetate) Tablets Recalled by Warner Chilcott...

The Issue: Failed Impurity/Degradation Specifications due to moisture ingress in...

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

Class III — Low RiskOngoing
Refund
DrugDecember 21, 2012· Warner Chilcott Company LLC

Recalled Item: Femtrace 0.9 mg (Estradiol Acetate) Tablets Recalled by Warner Chilcott...

The Issue: Failed Impurity/Degradation Specifications due to moisture ingress in...

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

Class III — Low RiskOngoing
Refund
FoodDecember 21, 2012· NBTY Inc.

Recalled Item: PURE PROTEIN PROTEIN SHOT 25g PROTEIN Recalled by NBTY Inc. Due to...

The Issue: Lactobacillus plantarum and Lactobacillus brevis were detected in a sample...

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

Class III — Low RiskOngoing
Refund
FoodDecember 21, 2012· NBTY Inc.

Recalled Item: MET-Rx EXTREME THERMO RAGE WATERMELON DIETARY SUPPLEMENT Recalled by NBTY...

The Issue: Acetobacter lovaniensis was detected in a sample of the product tested by a...

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

Class III — Low RiskOngoing
Refund
FoodDecember 21, 2012· Dollar Tree Distribution, Inc.

Recalled Item: Candy Canes Recalled by Dollar Tree Distribution, Inc. Due to Candy product...

The Issue: Candy product may contain metal and/or plastic pieces embedded in the candy.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2012· Dollar Tree Distribution, Inc.

Recalled Item: Candy Canes Recalled by Dollar Tree Distribution, Inc. Due to Candy product...

The Issue: Candy product may contain metal and/or plastic pieces embedded in the candy.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 21, 2012· NordicNeuroLab AS

Recalled Item: nordicBrainEX Product Usage: nordicBrainEx is an image processing software...

The Issue: There is an error related to the relative geometry between fiber tracts in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2012· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR Recalled by Johnson &...

The Issue: Limited number of individual contact lens packages may not have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2012· Johnson & Johnson Vision Care, Inc.

Recalled Item: 1-DAY ACUVUE MOIST Brand Contact Lenses Recalled by Johnson & Johnson Vision...

The Issue: Limited number of individual contact lens packages may not have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog...

The Issue: Reports of handle fracture and subsequent disassociation of cam assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Abbott Medical Optics Inc (AMO)

Recalled Item: AMO Sensar Intraocular Lenses (IOLs) Recalled by Abbott Medical Optics Inc...

The Issue: Two production orders of these IOLs that contain mislabeled IOLs.

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

Class II — Potential Health HazardOngoing