All recall categories

Recalls distributed in Massachusetts

These notices name Massachusetts 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.

4,249 stored notices name Massachusetts, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Massachusetts too — those are in the archive.

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100…

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

Covidien, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Hamilton Microlab STAR Liquid Handler; Protocol Configuration Tool (PCT) v2.0.0. Used to conduct F1CDx and F1LCDx.

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

Foundation Medicine, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Gifford's HomeMaine ice cream brand POWER PLAY FUDGE; ONE QUART (946 mL); UPC: 8 60864 00030 7

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

Gifford's Dairy, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200…

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

Kico Knee Innovation Company

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Protein Cereal Cocoa Crunch. Shelf stable, ready to eat cereal product. 25-year shelf life, metalized poly pillow…

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

Nutrient Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001

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

Paragonix Technologies Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2026Updated Sep 7, 2026

Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

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

Prospector Popcorn, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2026Updated Sep 7, 2026

Dentsply Sirona Capsule Mixer Model No. 5546068

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

SDI Limited

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 26, 2026

Shanghai Ravioli Corporation Recalls Not Ready-To-Eat Frozen Buffalo Chicken Products Produced Without the Benefit of…

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

Shanghai Ravioli Corporation

USDA FSIS

Food

Reported Aug 19, 2026Updated Sep 7, 2026

Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with…

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

529 Commerce, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2026Updated Sep 7, 2026

ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000

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

Erbe USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1

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

OBP Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102 Software Version: N/A Product…

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

Spacelabs Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

GM Helix Implant, Endosseous Dental Implant Article No. 109.984

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

Straumann USA LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 19, 2026Updated Sep 7, 2026

MARKETSIDE ICEBERG SALAD 10/24 oz, UPC 681131328951; MARKETSIDE ICEBERG SALAD 12/12 oz, UPC 681131328944; MARKETSIDE…

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

Taylor Farms de Mexico S. de R.L. de C.V.

20 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2026Updated Aug 25, 2026

navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material…

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

Ventana Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US), Electronic installed on the following instruments: -…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

FilmArray NGDS Warrior Panel REF NGDS-ASY-0007 UDI-DI code: (01)00851458005136 The FilmArray NGDS Warrior Panel is a…

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

Biofire Defense

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Radial Jaw 4 Standard Capacity Biopsy Forceps with the following descriptions and UPN: 1. Radial Jaw 4 SC 240cm Box 20;…

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

Boston Scientific Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

HardyDisk AST Cefiderocol 30¿g (FDC30) REF Z9435 HardyDisk AST Cefiderocol 30¿g (FDC30) for in vitro agar diffusion…

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

Hardy Diagnostics

FDA (openFDA device enforcement)

Consumer products

Reported Aug 12, 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 Aug 12, 2026

Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530…

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

Maquet Critical Care AB

FDA (openFDA device enforcement)

Medical devices

Reported Aug 12, 2026

Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…

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

Pride Mobility Products Corp.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 5, 2026

L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x…

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

Argon Medical Devices, Inc.

1 more product 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.