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. 2,336 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,336 in last 12 months

Showing 2996129980 of 46,762 recalls

Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: Mucosal Atomization Device (MAD) Recalled by Teleflex Medical Due to Product...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADomizer Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADdy Recalled by Teleflex Medical Due to Product Defect; These products...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADett Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: FLEXI NOZZLE LONG Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: FLEXI NOZZLE SHORT Product Usage: These products are used for Recalled by...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADgic Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2016· Ortho-Clinical Diagnostics

Recalled Item: VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 Recalled by...

The Issue: CRP samples diluted using VITROS Chemistry Products Specialty Diluent,...

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

Class III — Low RiskOngoing
Medical DeviceOctober 26, 2016· 3M Company - Health Care Business

Recalled Item: 3M Universal Electrosurgical Pad Recalled by 3M Company - Health Care...

The Issue: 3M is recalling Universal Electrosurgical Pads because a report of an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...

The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· Exactech, Inc.

Recalled Item: Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit Recalled by...

The Issue: Disengaged screw head could potentially not be retained in the Torque...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT Recalled...

The Issue: Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2016· Trumpf Medical Systems, Inc.

Recalled Item: OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has...

The Issue: Trumpf has identified six incidents of pinched cables.

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

Class II — Potential Health HazardOngoing
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: UROPHEN MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: UROLET MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: AZUPHEN MB URINARY ANTISEPTIC Capsules Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: URAMIT MB URINARY ANTISEPTIC Capsules Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Hyolev MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund