All recall categories

Recalls distributed in Maine

These notices name Maine 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.

1,801 stored notices name Maine, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Maine too — those are in the archive.

Food

Reported Jul 22, 2026

Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl.…

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

Amy's Kitchen Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 22, 2026

Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4.…

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

General Mills James Ford Bell Technical Center

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 22, 2026

da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2026

functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ…

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

Nutricia North America

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 15, 2026

Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

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)

Food

Reported Jul 8, 2026

MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a…

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

Mars Snacking

1 more product in this recall

FDA (openFDA food enforcement)

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

Da Vinci ASSY, PSS, SP1098, Part Number: 380601

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

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)

Food

Reported Jul 1, 2026

1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.

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

Utz Quality Foods, LLC

5 more products in this recall

FDA (openFDA food enforcement)

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)

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

Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669 00884450529690 REF:…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Mito Red Light, Super Mobile

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

Mito Red Light Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US…

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

Thoratec LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 24, 2026

Great Value Hawaiian Roll 4pk, Item # F63384. Product is perishable dinner roll ready to eat, sold in a corrugated case…

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

United States Bakery

FDA (openFDA food 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

Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ…

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

Kettle Cuisine, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 10, 2026

Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description:…

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

Baxter Healthcare Corporation

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.