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 Jul 8, 2026

OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI…

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

Bard Access Systems, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the…

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1…

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

Hamilton Medical AG

1 more product in this recall

FDA (openFDA device enforcement)

Consumer products

Reported Jul 8, 2026Updated Sep 16, 2026

Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…

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

KAO USA Inc.

FDA (weekly enforcement report)

Medical devices

Reported Jul 8, 2026

Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…

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

Teleflex LLC

FDA (openFDA device enforcement)

Drugs

Reported Jul 1, 2026Updated Sep 16, 2026

Determine HIV 1/2 Ag/Ab Combo 25T, Model/Catalog No. 7D2648

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

Abbott Diagnostics Scarborough, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Jul 1, 2026

INZONE DETACHMENT SYSTEM, REF: M00345100950

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Meat & poultry

Reported Jun 25, 2026

FSIS Issues Public Health Alert for Boneless Chicken Breast Product Due to Misbranding and Undeclared Allergens

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

FW Farms LLC.

USDA FSIS

Medical devices

Reported Jun 24, 2026

PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU

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

Arrow International, LLC

34 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 24, 2026

azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF JAPAN DISTRIBUTED BY: AZUMA…

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

Azuma Foods International Inc. USA

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2026

BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

iLet Bionic Pancreas, REF: BB1001

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

Beta Bionics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR ICL…

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

Staar Surgical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jun 17, 2026

Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software

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

Abbott Medical

FDA (openFDA device enforcement)

Food

Reported Jun 17, 2026

DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz (125 g) PRODUCT OF THAILAND Packed for: U.S. Trading Company Hayward,…

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

U.S. Tov, Inc. dba U.S. Trading Company

FDA (openFDA food enforcement)

Medical devices

Reported Jun 10, 2026

BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose…

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

Becton Dickinson & Company

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 10, 2026

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 TOWER,IS5000 Model/Catalog Number: 380746 Software Version: N/A Product…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 10, 2026

Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 /…

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

Shimadzu Medical Systems

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2026

Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…

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

Becton, Dickinson and Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2026

Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley…

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

C.R. Bard Inc.

FDA (openFDA device enforcement)

Food

Reported May 27, 2026

GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry…

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

Ghirardelli Chocolate Company

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 20, 2026

Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…

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

Dexcom, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product…

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

Djo, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 13, 2026

ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…

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

Erbe Medical, LLC

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.