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 48,122 notices were distributed nationwide, so they reach Massachusetts too — those are in the archive.

Medical devices

Reported Feb 13, 2019

NeuViz 128 Multi-slice CT Scanner System with software version 1.0.8.5010O+P04 Vi .0.8.521 9+PO1 Multi-Slice CT Scanner…

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

Neusoft Medical Systems Imp & Ex

FDA (openFDA device enforcement)

Food

Reported Feb 13, 2019

Chicago's Pizza Base Mix, Manufactured Exclusively for Chicago's Pizza, Greenfield, IN packaged in 30 lb bags.

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

Pizza Blends, LLC

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 13, 2019

Product: ABL800 FLEX with Crea. The ABL800 with Crea is available in the following configurations: ABL817, ABL827 and…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2019

Meiqili Durian Candy in plastic bag with clear window, Net Wt: 12 ounce (340 g). It is a labeled as a product of P.R.C.…

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

Fine Land Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2019

Cell Saver 5/5+ Bowl Set, 70ml, Product ID: 0291E-00, 0291A-00 Indications for Use: The Haemonetics Cell Saver 5/5+…

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

Haemonetics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 6, 2019

Peaches, sold as a bulk retail item, with PLU 4044, and country of origin of Chile. The peaches sold at Aldi are…

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

Jac Vandenberg Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 6, 2019

New & Improved RTU Donut Glaze, NET WEIGHT 2800 lb. (1270 Kg) tote, UPC Codes: 608002213109, Product Code: 4110531

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

Pennant Ingredients

FDA (openFDA food enforcement)

Medical devices

Reported Jan 30, 2019

Perfusion Pack, Rx only, Sterile EO

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

LivaNova USA

FDA (openFDA device enforcement)

Meat & poultry

Reported Jan 28, 2019

Perdue Foods, LLC Recalls Refrigerated Fun Shapes Chicken Breast Nuggets Due to Misbranding and Undeclared Allergens

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

Perdue Foods, Llc.

USDA FSIS

Medical devices

Reported Jan 23, 2019

Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2019

U by Kotex¿ Sleek¿, Regular Tampons, 18 Count

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

Kimberly-Clark Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2019

DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray…

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

Agfa-Gevaert, N.V.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2019

Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2019

ddRCombi Plus FP, Model Number 8.2000.0070.0 (US Version), 8.2000.0060.0 (Europe Version) The ddRCombi Plus FP is a…

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

Swissray Medical AG

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

Quantikine¿ IVD¿ ELISA, Human sTfR Immunoassay kit. Product Usage: The QuantikineTM IVDTM sTFR Enzyme linked…

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

R & D Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

GEM Coupler Forceps, GEM4183C, packaged individually.

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

HydroSet XT Injectable HA Bone Cement, REF 897003, STERILE

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

Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit per Cavity #3 Cavity Deep/20 pieces per case…

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

ICU Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Laparotomy Sponge, XR No Loop, Single-Use, Sterile, 18'' x 18'' pre-washed with bands without handles, 5 sponges/pack,…

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

Medical Action Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G…

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

Medtronic Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6, RayStation 7 and RayStation…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Food

Reported Jan 2, 2019

ROOT 23 CUCUMBER HABANERO SIMPLE SYRUP 375 ml

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

Root 23 LLC

FDA (openFDA food 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.