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. 2,374 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,374 in last 12 months

Showing 2200122020 of 46,762 recalls

DrugFebruary 6, 2019· Advanced Pharma Inc.

Recalled Item: Oxytocin 20 Units added to NS 1000 mL (oxytocin and Recalled by Advanced...

The Issue: Superpotent Drug: product may contain concentrations of oxytocin higher than...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 6, 2019· Advanced Pharma Inc.

Recalled Item: Oxytocin 30 Units added to NS 500 mL (oxytocin and Recalled by Advanced...

The Issue: Superpotent Drug: product may contain concentrations of oxytocin higher than...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 6, 2019· Advanced Pharma Inc.

Recalled Item: Oxytocin 10 Units added to NS 1000 mL (oxytocin and Recalled by Advanced...

The Issue: Superpotent Drug: product may contain concentrations of oxytocin higher than...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 6, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules USP Recalled by Dr. Reddy's...

The Issue: Discoloration: Esomeprazole Magnesium DR Capsules (40mg) may contain brown...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 6, 2019· Medica Corporation

Recalled Item: Medica Wash1-Wash solution used prior to Lipase assay on the Recalled by...

The Issue: Wash1 solution is ineffective in cleaning dispensing probe of TRIG and LDL...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2019· LW Scientific, Inc.

Recalled Item: LW Scientific ZIP IQ PCV Centrifuge Recalled by LW Scientific, Inc. Due to...

The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2019· LW Scientific, Inc.

Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...

The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2019· LW Scientific, Inc.

Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...

The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2019· Abbott Ireland Diagnostics Division

Recalled Item: Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT...

The Issue: Patient results may be falsely elevated. This patient impact only applies to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2019· Abbott Ireland Diagnostics Division

Recalled Item: Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity Recalled by...

The Issue: Patient results may be falsely elevated. This patient impact only applies to...

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

Class II — Potential Health HazardOngoing
DrugFebruary 4, 2019· Akorn Inc

Recalled Item: Moisturizing Lubricant Eye Drops Recalled by Akorn Inc Due to Failed...

The Issue: Failed Stability Specification: out of specification results for Sodium...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 4, 2019· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2019· CP Medical Inc

Recalled Item: Plain and Chromic Gut Absorbable Surgical Sutures Recalled by CP Medical Inc...

The Issue: Potential compromise of product sterility after routine monitoring for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2019· US Endoscopy Group Inc

Recalled Item: US Endoscopy Padlock Clip defect closure system The Recalled by US Endoscopy...

The Issue: Potential esophageal laceration during a patient procedure

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

Class II — Potential Health HazardOngoing
DrugFebruary 1, 2019· Mylan Institutional Inc

Recalled Item: Levoleucovorin Injection Recalled by Mylan Institutional Inc Due to Presence...

The Issue: Presence of Particulate Matter: particulate matter identified as copper salts

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 1, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray...

The Issue: Defective Container: Potential for broken glass in the neck area of the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 1, 2019· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...

The Issue: Potentially comingled, resulting in the product in the box potentially not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2019· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...

The Issue: Potentially comingled, resulting in the product in the box potentially not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2019· Cook Inc.

Recalled Item: Cook Transseptal Needle Recalled by Cook Inc. Due to The products were...

The Issue: The products were manufactured without a back bevel on the needle tip. This...

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

Class I — Serious Health HazardOngoing
DrugJanuary 31, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications: Out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund