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 4380143820 of 46,762 recalls

Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: Pump shutting off during use without warning.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling

The Issue: Product may be mislabeled.

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

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

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: Pump shutting off during use without warning.

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

Class I — Serious 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
Medical DeviceMarch 18, 2013· LeMaitre Vascular, Inc.

Recalled Item: Glow 'N Tell 20 cm Tape: 1100-00 (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· Integra Burlington MA, Inc.

Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....

The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...

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

Class II — Potential Health HazardOngoing
DrugMarch 16, 2013· Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals

Recalled Item: "Well at Wallgreens" Regular Strength Antacid Liquid...

The Issue: Microbial Contamination of Non-Sterile Products: Lot in question had an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Lessina(R) (Levonorgestrel and ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Errin (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Junel(TM) Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camila (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Jolessa(R) (levonorgestrel/ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Balziva(TM) (norethindrone and ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2013· MCKESSON TECHNOLOGIES INC.

Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...

The Issue: There was an occurrence where the patient case data did not match the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Intuitive Surgical, Inc.

Recalled Item: IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical Recalled by...

The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Intuitive Surgical, Inc.

Recalled Item: IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System...

The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Acist Medical Systems

Recalled Item: ACIST Medical Systems Inc. The ACIST Angiographic Injection System is...

The Issue: ACIST Medical Systems is issuing a voluntary recall notice for three...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· AGFA Corp.

Recalled Item: IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound...

The Issue: Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV...

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

Class II — Potential Health HazardOngoing