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.

4,307 stored notices name Massachusetts, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Massachusetts too — those are in the archive.

Food

Reported Apr 23, 2025

LEMON PLUM; NET WT: 228G (8oz); INGREDIENTS: Plum, sugar, salt, lemon juice, food additives (citric acid, sodium…

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 Apr 23, 2025

Guide Wire with Ruler Tube 3x800 mm DIA; Catalog number/REF: 2351-3080S;

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

Stryker GmbH

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 23, 2025

HeartMate Mobile Power Unit: REF: 107754, NA; 107758, EU; 107758AU, AU; 107758UK, UK; L107758, EU Rental. Used with…

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

Thoratec LLC

FDA (openFDA device enforcement)

Food

Reported Apr 23, 2025

BaiWei ShanZhuang, Dried Seedless Plum Candy, 9.16 oz. (260g), plastic bags, 30 bags per case.

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

Tristar Food Wholesale Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 16, 2025

GenetiSure Dx Labeling Kit, REF: K1201-64105, contains human reference DNA female aliquot, REF5190-7317. A required kit…

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

Agilent Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 16, 2025

BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex, BD Pyxis" MedBank" MedPass are automated…

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 16, 2025

Dr. Praeger s California Veggie Fries 8oz,

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

Dr. Praeger's Sensible Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 16, 2025

Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration Tubing, REF: APT6072-132. Hippo 072…

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

Qapel Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 16, 2025

stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless Steel, Catalog Number MRUE200, packaged in…

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

Tornier S.A.S.

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 16, 2025

Dried Cranberries (21.75 lb/case; 300 - 1.16 oz packages/case)

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

Victor Packing Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 9, 2025

BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Apr 9, 2025

DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 9, 2025

Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a…

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

Nestle-USA, Inc. (Corporate Office)

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 9, 2025

Boppli: Bedside Device Kit, REF: 54-0002; Sensor Band, REF: 51-0007

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

Pyrames Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 9, 2025

Brand Name: QIAstat-Dx Product Name: QIAstat-Dx Respiratory Panel Plus Reference Number (REF): 691224 Software Version:…

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 9, 2025

Monterey AL Implant Inserter; 10/12mm; Catalog 48019100.

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

Stryker Spine

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 2, 2025

CVAC Aspiration System, REF: CVC127020-1, and User Manual L00018. Intended for endoscopic examination/treatment of…

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

Calyxo, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 2, 2025

Jinga Glass Noodles with vegetables 8 oz. and 12 oz.

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

HAR Maspeth Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 2, 2025

CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital System Model CM3100 -CardioMEMS Backend Web…

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

St. Jude Medical

FDA (openFDA device enforcement)

Medical devices

Reported Apr 2, 2025

NexGen LPS Flex, Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis, Model…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF:…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.

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

FUJIFILM Healthcare Americas Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H…

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

Oridion Medical 1987 Ltd.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2025

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software…

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

Intuitive Surgical, 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.