All recall categories

Recalls distributed in Alaska

These notices name Alaska in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

1,282 stored notices name Alaska, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Alaska too — those are in the archive.

Medical devices

Reported Mar 13, 2024

ConvaTec Natura Stomahesive Post-Operative / Surgical Ostomy System, REF 416938, 1 3/4 in. 45mm, Sterile.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ConvaTec, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Mar 13, 2024

Taylor Farms Pacific Recalls Kroger Brand Ready-To-Eat Apple Walnut With Chicken Salad Bowl Products Due to Misbranding…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Taylor Farm - Pacific

USDA FSIS

Food

Reported Mar 6, 2024

Rojo Black Bean 6 Layer Dip packaged in 20oz PET plastic containers, sold in sleeve with two containers per sleeve. 12…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lakeview Farms LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2024

BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2024

Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

U.S. Tov, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 14, 2024

Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 31, 2024

PANTHER FUSION System REF 9121010000 The Panther System is an integrated nucleic acid testing system which fully…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hologic, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 24, 2024

Ministry of Snacks Sweet and Savory Collection #8700

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Houdini Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 17, 2024

Alinity i Processing Module REF 03R65-01 The Alinity i Processing Module is a fully automated immunoassay analyzer…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Navigation, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Respironics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

Alinity ci-series System Control Module, REF: 03R70-01

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

Injection Needle, REF: 25207

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Karl Storz Endoscopy

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Nurse Assist, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Physio-Control, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 27, 2023

HMC Farms Peaches 2lb Gusset Bag

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The HMC Group Marketing Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 20, 2023

Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Houdini Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 20, 2023

TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

Monarch Platform REF MON-000005-01, 100-240V- 50/60Hz 1440w

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Auris Health Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 13, 2023

STAT-Site M BHB Test Strips, used with STAT-SITE M Beta-HB Meter as an in vitro diagnostic for blood ketone values.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stanbio Laboratory, LP

FDA (openFDA device enforcement)

Medical devices

Reported Dec 6, 2023

Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.