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 29, 2025

BD PCR Cartridges used with MAX System. Model Number: 437519

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

McKesson Cardiology Hemo software

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

A L I Technologies Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…

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

Alcon Research LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Panther Fusion GBS Assay REF PRD-04484 Kit containing Panther Fusion GBS Reagent Cartridge IVD.

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

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179

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

Intuitive Surgical, Inc.

38 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810,…

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

Mercury Enterprises, Inc. dba Mercury Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2025

Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.

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

Spacelabs Healthcare, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2025

3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self…

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

3M Unitek Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…

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

Straight Smile, LLC

FDA (openFDA device enforcement)

Food

Reported Jan 1, 2025

ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch

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

Zoe US, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 25, 2024

Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 18, 2024

BD Pyxis MedStation ES, REF: 323

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2024

Fresh Gourmet TORTILLA STRIPS SANTA FE SYTLE NET WT 3.5 OZ (99g) UPC 7 87359 17504 6 DISTRIBUTED BY: FRESH GOURMET CO.…

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

Sugar Foods LLC

FDA (openFDA food enforcement)

Food

Reported Dec 11, 2024

(1) READY MEALS GREEN CHILI CHICKEN ENCHILADAS SS COLD (UPC 21291600000) (2) GREEN CHICKEN ENCHILADAS 6 CT SS COLD (UPC…

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

Albertsons Companies LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2024

Curio Spice Co. brand Grains of Paradise (Korerima) - Jar 1.25 oz net wt. UPC: 672975171032

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

Curio Spice Co.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2024

V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an…

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

Kci USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2024

Hannaford brand seafood salad; Net Wt. 12 oz. (340g); INGREDIENTS: SEAFOOD BLEND (FISH PROTEIN [ALASKA POLLOCK AND/OR…

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

R. Walters Foods, Limited Liability Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Nov 20, 2024

The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component:…

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

Draeger Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog Number: WA22810A Software Version: N/A Product…

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

Olympus Corporation of the Americas

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Trilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B,…

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

Philips Respironics, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to…

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

Percussionaire Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

Item 407118, UPC 13454 38493, Bistro 28 Creamy Green Chile Chicken Enchilada Express Meal Kit. Make 6 Enchiladas. Ready…

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

Reser's Fine Foods, Inc.

17 more products in this recall

FDA (openFDA food 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.