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. 2,435 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,435 in last 12 months

Showing 1824118260 of 46,762 recalls

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· 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· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio Recalled by Siemens Medical Solutions USA, Inc Due to The Ysio system...

The Issue: The Ysio system may process incorrect internal values for the position of...

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· Covidien Llc

Recalled Item: Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed...

The Issue: Sterile packaging may potentially be compromised, and use of products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2020· Covidien Llc

Recalled Item: Covidien Force TriVerse Electrosurgical Devices Recalled by Covidien Llc Due...

The Issue: Sterile packaging may potentially be compromised, and use of products may...

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

Class II — Potential Health HazardOngoing
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· 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
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
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 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 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
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 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
Medical DeviceFebruary 4, 2020· Wilson-Cook Medical Inc.

Recalled Item: HEMO-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....

The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2020· Wilson-Cook Medical Inc.

Recalled Item: HEMO-10 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....

The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...

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

Class II — Potential Health HazardOngoing