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. 1,785 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,785 in last 12 months

Showing 2548125500 of 46,762 recalls

DrugJanuary 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Mitomycin 40 mg/mL Preservative Free Irrigation Volume: 10 mL SDV Recalled...

The Issue: Labeling: Label Error on Declared Strength

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2018· Time-Cap Laboratories, Inc.

Recalled Item: Ibuprofen Tablets USP 600 mg Recalled by Time-Cap Laboratories, Inc. Due to...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2018· Ethicon, Inc.

Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...

The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2018· Riverpoint Medical, LLC

Recalled Item: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint...

The Issue: Product is labeled with "CE", but is not yet approved in the European Union.

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

Class III — Low RiskOngoing
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2018· Marksans Pharma Inc.

Recalled Item: Ibuprofen Tablets Recalled by Marksans Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 4, 2018· International Laboratories, LLC

Recalled Item: Clopidogrel Tablets Recalled by International Laboratories, LLC Due to...

The Issue: LABELING: LABEL MIX-UP. Simvastatin tablets, USP 10 mg were found in bottles...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 4, 2018· Toshiba American Medical Systems Inc

Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...

The Issue: The power supply unit may be damaged and may fail to start up when the power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...

The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2018· bioMerieux, Inc.

Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...

The Issue: Increase of events affecting performance regarding pump clogging and...

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

Class II — Potential Health HazardOngoing
FoodJanuary 4, 2018· Ventura Foods Llc

Recalled Item: SunGlow Recalled by Ventura Foods Llc Due to Undeclared Soy

The Issue: SunGlow contains undeclared soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 4, 2018· Ventura Foods Llc

Recalled Item: SunGlow Recalled by Ventura Foods Llc Due to Undeclared Soy

The Issue: SunGlow contains undeclared soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 3, 2018· Fieldbrook Foods Corporation

Recalled Item: Ice Cream Variety Packs containing Sandwiches Recalled by Fieldbrook Foods...

The Issue: Product may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund