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.

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 31, 2024

Vermont Village Unsweetened Apple Sauce (24oz)

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

Stonewall Kitchen, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 24, 2024

PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number…

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

Becton Dickinson & Company

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 24, 2024

INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040

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

Phase Scientific International Limited

FDA (openFDA device enforcement)

Food

Reported Jan 24, 2024

Wellsley Farms Assorted Mini Quiches NET WT 36 OZ (2LB 4 OZ) 1.02kb Keep Frozen UPC: 8867002630. Packaged in plastic…

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

The Fillo Factory Inc.

FDA (openFDA food enforcement)

Food

Reported Jan 24, 2024

Chicken Broth sold under Chef's Cupboard, 32oz Chicken Stock, UPC: 4099100067699, carton Gold Emblem, 32oz Chicken…

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

TreeHouse Foods, Inc.

14 more products in this recall

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)

Food

Reported Jan 17, 2024

Shiloh Farms Bread for Life Organic 7 Grain UPC 0-47593-02812-7

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Garden Spot Foods, LLC.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 17, 2024

Incisive CT, model 728143 & 728144 running Software Version 5.0.0.

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

Philips Healthcare (Suzhou) Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010,…

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

Townsend Design

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

Reverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797

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

Encore Medical, LP

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only

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

Natus Medical Incorporated

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

AcuMatch Hip System, Catalog Number 142-32-27

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

Exactech, Inc.

11 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

The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into…

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

Philips North America LLC

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)

Medical devices

Reported Dec 20, 2023

RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.

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

Encore Medical, LP

FDA (openFDA device 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

CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP)…

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

Integra LifeSciences Corp.

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)

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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.