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. 987 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
987 in last 12 months

Showing 18241–18260 of 46,762 recalls

Medical DeviceFebruary 10, 2020· Medline Industries Inc

Recalled Item: Medline Winged Sponges Presaturated W/PVP DYND70289H Expiration 06/30/2022....

The Issue: Voids were discovered in the packaging seal and loss of sterility on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Agfa N.V.

Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- Recalled...

The Issue: Tomosynthesis image acquisition sequence did not stop automatically after...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Medline Industries Inc

Recalled Item: Medline Sterile 3mL Syringes with 21GA x 1 Inch Needle Recalled by Medline...

The Issue: Voids were discovered in the packaging seal and loss of sterility on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Getinge 88-Series-washer disinfectors intended for cleaning Recalled by...

The Issue: Potential leakage that may occur due to ruptured spot welds in the chamber,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: McKesson Cardiology ECG Management Recalled by CHANGE HEALTHCARE CANADA...

The Issue: Inaccurate estimation of the heart rate may occur in instances where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Medline Industries Inc

Recalled Item: Medline Stick Sponge Presaturated W/PVP DYND70288H 2/PK Expiration Recalled...

The Issue: Voids were discovered in the packaging seal and loss of sterility on the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 10, 2020· Par Pharmaceutical Inc.

Recalled Item: Frovatriptan Succinate Tablets Recalled by Par Pharmaceutical Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Product incorrectly...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 7, 2020· AuroMedics Pharma LLC

Recalled Item: Amoxicillin and Clavulanate Potassium Tablets Recalled by AuroMedics Pharma...

The Issue: Presence of Foreign Substance: Customer complaint of a foreign substance...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 7, 2020· American Health Packaging

Recalled Item: Desmopressin Acetate Tablets Recalled by American Health Packaging Due to...

The Issue: GMP Deviations: Product bottle may be absent of desiccant.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 7, 2020· American Health Packaging

Recalled Item: Desmopressin Acetate Tablets Recalled by American Health Packaging Due to...

The Issue: GMP Deviations: Product bottle may be absent of desiccant.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 7, 2020· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Phenytoin Oral Suspension USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Resuspension Problems: Two lots of Phenytoin Oral Suspension USP 125mg/5mL...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 7, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys CA 19-9 Recalled by Roche Diagnostics Operations, Inc. Due to The...

The Issue: The firm has received an increased number of complaints concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2020· Integra LifeSciences Corp.

Recalled Item: NeuraGen Nerve Guide Recalled by Integra LifeSciences Corp. Due to...

The Issue: Nonconforming product which was dispositioned for rejection was mistakenly...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 6, 2020· Invivo Corporation

Recalled Item: Monitor for the Functional Imaging System for Magnetic Resonance Imaging...

The Issue: Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 Recalled by...

The Issue: Due to high discordant Estradiol results which.potentially affects all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and Recalled by...

The Issue: Due to high discordant Estradiol results which.potentially affects all...

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

Class II — Potential Health HazardOngoing
DrugFebruary 5, 2020· Pfizer Inc.

Recalled Item: Caduet (amlodipine besylate/atorvastatin calcium) Tablets Recalled by Pfizer...

The Issue: Defective Container: products potentially could have been packaged in...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2020· Pfizer Inc.

Recalled Item: Caduet (amlodipine besylate/atorvastatin calcium) Tablets Recalled by Pfizer...

The Issue: Defective Container: products potentially could have been packaged in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2020· CareFusion 303, Inc.

Recalled Item: CareFusion Alaris System Recalled by CareFusion 303, Inc. Due to 1)Error...

The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2020· CareFusion 303, Inc.

Recalled Item: CareFusion Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to...

The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...

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

Class I — Serious Health HazardOngoing