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.

Food

Reported Aug 16, 2023

Romaine lettuce packed in bulk 45-lb mini-bins

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

C&E Farms, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 16, 2023

HoverMatt, 39" W x 78" L, REF: HM39SPU-B

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2023

Impella RP Flex with SmartAssist intracardiac microaxial blood pump, Product Number 1000323

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

Abiomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2023

OEC Flexiview 8800 Systems with 9-inch Image Intensifier

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

GE OEC Medical Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 9, 2023

Plantation Candies Petite Misty Mints 10 lbs and 25 lb boxes Packaged in plastic bags inside cardboard boxes

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

Plantation Candies, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 9, 2023

The following Pro.specta Emission Computed Tomography Systems that were manufactured with an SLD Look Ahead Optical…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2023

Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral Femoral Plate 6 holes 159 mm Length-Indicated for temporary…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

Ringed DxI Reaction Vessels (RVs)

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…

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

Hamilton Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 2, 2023

FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA,…

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

Microvention Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 26, 2023

1/2 gallon CN Smith brand Apple Cider; 1/2 gallon and 16 oz. Wilson Farms brand Apple Cider; 1 gallon, 1/2 gallon, and…

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

Bevovations, LLC

FDA (openFDA food enforcement)

Food

Reported Jul 26, 2023

Romaine lettuce packed in bulk 45 pound mini-bins

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

C&E Farms, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 26, 2023

Simplexa Direct Amplification Disc Kit, Rx Only, IVD The Simplexa Direct Amplification Disc Kit, REF: MOL1455 is 1 box…

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

DiaSorin Molecular LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2023

Digisonics OBView Versions 4.8.2 SP6 - 4.8.3, Ultrasound reporting software

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

Digisonics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 26, 2023

Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…

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

Medtronic Neurosurgery

FDA (openFDA device enforcement)

Food

Reported Jul 19, 2023

Tampico brand Mango Punch; LESS THAN 1% JUICE; 1 GAL (3.78 L); INGREDIENTS: WATER, HIGH FRUCTOSE CORN SYRUP, LESS THAN…

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

Garelick Farms LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 19, 2023

HeartSine, REF: PAD-PAK-01, PAD-PAK-03 AND PAD-PAK-03j, CE0123 sold separately and with the HeartSine Samaritan Public…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 12, 2023

Cricket Creek Farm brand Sophelise cheese

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

Cricket Creek Farm LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 12, 2023

da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU,…

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

Quidel Cardiovascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 12, 2023

Aptio Automation Storage and Retrieval Module (SRM)

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 5, 2023

1. VIT-RA-TOX Calphonite #38, 15 Fl. oz. (444 ml) in an amber glass bottle; 2. Sonne's Calphonite #2, 15 Fl. oz. (444…

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

Anatox Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 5, 2023

Access Hybritech p2PSA reagent, REF B03704 and REF A49752.

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

Beckman Coulter, Inc.

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.