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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 Jun 8, 2022

XVIVO Organ Chamber REF 19020

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

Xvivo Perfusion Ab

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V

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

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with…

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

Medtronic Neuromodulation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray with a snap on…

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

Medtronic Perfusion Systems

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2022

(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732,…

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

Teleflex Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

Dragonfly OpStar Imaging Catheter, REF 1014651/1014652, 0.068 in, 0.014 in, 135 cm, STERILE EO

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

Abbott Vascular

FDA (openFDA device enforcement)

Medical devices

Reported May 25, 2022

Getinge 9100-Series Washer Disinfector models: 9120E, 9125E, 9127E, 9128E, 9122EW, 9128EW.

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

Getinge USA Sales Inc.

FDA (openFDA device enforcement)

Food

Reported May 25, 2022

Gorton s Fish Sandwich Fillets, 18.3 OZ, UPC 44400 15440

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

Gorton's, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 25, 2022

Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v.…

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

Daavlin Distributing Company

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 18, 2022

Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ (250mL) UPC 8373726342 24 bottles per case

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

Eastland Food Corporation

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2022

11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (10-2018)

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

Karl Storz Endoscopy

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…

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

Medtronic Vascular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

Accula SARS-CoV-2 Test, REF: COV4100

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

Mesa Biotech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2022

ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test, and associated ProterixBio Dried Blood Spot Collection Kit, no model…

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

Proterixbio

FDA (openFDA device enforcement)

Food

Reported May 18, 2022

'KORICA' ROASTED PEANUT; 10.6OZ (300G); packaged in plastic bags; Ingredients: Peanuts, Salt, Licorice, Anise,…

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

Rong Shing Trading NY Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2022

OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143

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

Simplivia Healthcare Ltd.

FDA (openFDA device enforcement)

Food

Reported May 11, 2022

Olive; TOP SAVOR Licorice Flavored Olive; Net wt: 500g (17.63oz); Ingredients: olive, sugar, salt, licorice extract,…

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

A & C Best Food Trading

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 11, 2022

TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,

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

Johnson & Johnson Surgical Vision Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 4, 2022

ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.

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

Carl Zeiss Meditec AG

FDA (openFDA device enforcement)

Food

Reported May 4, 2022

Kinder Happy Moments Kinder Chocolate and Crispy Wafers Assortment 14.1 OZ (400g) square box with lid. Best by: July…

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

Ferrero USA Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 4, 2022

da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported May 4, 2022

Rebel Pistachio Ice Cream, one pint (473 mL, UPC 8 53149 00821 1, Manufactured by Rebel Creamery LLC, Midway, UT 84049.…

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

Rebel Creamery

FDA (openFDA food enforcement)

Medical devices

Reported May 4, 2022

TearCare version 1.0 SmartHubs

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

Sight Sciences, Inc.

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.