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 1818118200 of 46,762 recalls

FoodFebruary 21, 2020· Moonstruck Chocolate Company

Recalled Item: Moonstruck Praline Pecan & Ginger Element Bar in Dark Chocolate Recalled by...

The Issue: Undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 21, 2020· Epimed International

Recalled Item: R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496...

The Issue: Incorrect expiration date on introduction cannula packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Epimed International

Recalled Item: R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124...

The Issue: Incorrect expiration date on introduction cannula packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2020· Qiagen Sciences LLC

Recalled Item: AmniSure ROM Test Recalled by Qiagen Sciences LLC Due to An image on the...

The Issue: An image on the associated polybag contains an incorrect rinse time of 30...

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

Class II — Potential Health HazardOngoing
DrugFebruary 20, 2020· Teva Pharmaceuticals USA

Recalled Item: Mesalamine Delayed-Release Tablets Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Dissolution Specifications: Low out of specification dissolution...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2020· Radiometer Medical ApS

Recalled Item: TCM4 Base unit Recalled by Radiometer Medical ApS Due to Reports have been...

The Issue: Reports have been received about the transcutaneous monitoring system...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2020· Philips North America, LLC

Recalled Item: Expression MR400 MRI Patient Monitoring System Model Number: 866185 Software...

The Issue: Menu selections for users to access the oxygen (O2) sensor calibration were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2020· Haemonetics Corporation

Recalled Item: TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0...

The Issue: Software defect in TEG Manager impacts the displayed alert for out of range...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to Tests returning incorrect...

The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· James Leckey Design Ltd

Recalled Item: Firefly Floorsitter Recalled by James Leckey Design Ltd Due to The firm...

The Issue: The firm received reports of a number of broken latches on the floorsitter.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2020· Randox Laboratories Ltd.

Recalled Item: Chemistry QC Premium Plus Recalled by Randox Laboratories Ltd. Due to The...

The Issue: The control target and range value for Sodium using the ISE indirect method...

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

Class II — Potential Health HazardOngoing
DrugFebruary 17, 2020· Strides Pharma Science Limited

Recalled Item: Potassium Chloride Extended-Release Tablets USP Recalled by Strides Pharma...

The Issue: Failed Tablet/Capsules Specifications: Oversized tablets were found in one...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 17, 2020· Advanced Bionics, LLC

Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...

The Issue: hearing performance degradation due to body-fluid entering the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2020· Advanced Bionics, LLC

Recalled Item: AB HiResolution Bionic Ear System Recalled by Advanced Bionics, LLC Due to...

The Issue: hearing performance degradation due to body-fluid entering the device.

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

Class II — Potential Health HazardOngoing
FoodFebruary 14, 2020· Custom Foods LLC

Recalled Item: Sticky Fingers Bakeries Gluten-Free Scones Recalled by Custom Foods LLC Due...

The Issue: Firm received customer inquiry of why wheat is listed in the ingredient list...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 14, 2020· ICU Medical, Inc.

Recalled Item: The Cogent Hemodynamic Monitoring System. Recalled by ICU Medical, Inc. Due...

The Issue: Firm identified software issues which leads to the patient ID and patient...

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

Class II — Potential Health HazardOngoing