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 Aug 6, 2025

SafeStar 90 Plus Filter. Bidirectionally breathing system filter.

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

Draeger, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, used with HAMILTON-C1,…

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700,…

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

Volcano Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and…

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

CooperSurgical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N,…

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

Covidien

FDA (openFDA device enforcement)

Food

Reported Jul 30, 2025

Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside…

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

Mondelez Global LLC

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 30, 2025

Middle East Coast brand Tahini Dip; NET WT: 6 OZ (170g); INGREDIENTS: TAHINI, ORGANIC LEMON JUICE, GARLIC, OLIVE OIL,…

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

Shovel and Spoon LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 30, 2025

Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip

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

Stryker Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2025

Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog…

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

Alcon Research LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2025

Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model/Catalog Number: OPTI16 Software…

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

Edwards Lifesciences, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Jul 11, 2025

FSIS Issues Public Health Alert for Ready-To-Eat Pulled Pork Products Due to Misbranding and Undeclared Allergens

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

Roth Premium Foods, LLC

USDA FSIS

Medical devices

Reported Jul 9, 2025

BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF:…

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

C.R. Bard Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2025

HardyCHROM CRE, selective and differential culture medium for antimicrobial susceptibility testing, Product Catalog No.…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Food

Reported Jul 9, 2025

Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,…

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

Peak Cocktails

FDA (openFDA food enforcement)

Medical devices

Reported Jul 9, 2025

BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients…

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

Philips Respironics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164;…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

DxI 9000 Access Immunoassay Analyzer C11137

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2025

Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 2, 2025

FIREHOOK ARTISAN BAKED CRACKERS CLASSIC SEA SALT NET WT. 8 OZ (227g) INGREDIENTS: ORGANIC WHEAT FLOUR, ORGANIC HONEY,…

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

Firehook

FDA (openFDA food enforcement)

Medical devices

Reported Jun 25, 2025

Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851…

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

Balt USA, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite…

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

Bd Switzerland Sarl

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution

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

Contamac Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 18, 2025

Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…

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

Covidien

FDA (openFDA device enforcement)

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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.