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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.

4,307 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.

Medical devices

Reported Nov 27, 2024

MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue…

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

Ethicon, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 27, 2024

Douglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle. UPC # 10539 97452, Lot Numbers ,50335944…

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

Nestle Product Technology Center - Nestle Health Science

FDA (openFDA food enforcement)

Medical devices

Reported Nov 27, 2024

OrganOx metra -Intended as a Normothermic Machine Perfusion system of donor transport livers. Model/Catalog Number:…

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

OrganOx Ltd.

FDA (openFDA device enforcement)

Food

Reported Nov 27, 2024

Aldi Emporium Selection Brie 8oz UPC 4099100084016; 12 retail units per case La Bonne Vie Brie 8oz UPC 820581678531; 6…

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

Savencia Cheese USA

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 20, 2024

The EVSRF catheter is a sterile, single-use disposable medical device for endovenous radiofrequency ablation, a…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component:…

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

Draeger Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog Number: WA22810A Software Version: N/A Product…

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

Olympus Corporation of the Americas

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Trilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B,…

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

Philips Respironics, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

VYGON 100 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9601; An empty single-use pouch made of plastic intended to…

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

The Metrix Company

15 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2024

intelliPATH Universal HRP Detection Kit, REF: IPK5011G80, containing DAB Buffer, Catalog Number: IPBF5009G20; ONCORE…

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

Biocare Medical, LLC

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2024

Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged in a 4 oz (113g) Stand-Up Resealable Pouch. Item Number:…

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

Hammond's Candies Since 1920 II, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2024

Adult Cap-ONE Biteblock REF YG-227T The cap-ONE Biteblock is intended to sample CO2 and administer supplemental oxygen,…

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

Nihon Kohden America Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2024

Aunt Millie s Bakehouse Hawaiian Hamburger Buns 4.5" Sliced 3 OUNCE. 6 unlabeled 12CT PKGS per sale unit case, product…

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

Perfection Bakeries LLC

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2024

SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment is suitable for radiographic and fluoroscopic…

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

Shimadzu Corporation Medical Systems Division

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

Abbott Alinity m HPV AMP Kit, used with the Alinity m System, product codes: a) REF 09N15-095; b) REF 09N15-090; c) REF…

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

Abbott Molecular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

(Principal Display) ENOKI MUSHROOM Champignons d'enoki Net Wt: 150g (5.3oz) in a clear plastic packaged. (Back Display)…

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

Enoki King Mushroom Farm Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2024

Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor, 0.9m Model 809030006 Disp. SpO2 Forehead Probe, Adult,…

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

Nihon Kohden America Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to…

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

Percussionaire Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

LIFEPAK 15 (LP15) Model/Catalog Numbers: o 97577-000101 o 99577-000046 o 99577-000055 o 99577-000061 o 99577-000076 o…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

Item 407118, UPC 13454 38493, Bistro 28 Creamy Green Chile Chicken Enchilada Express Meal Kit. Make 6 Enchiladas. Ready…

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

Reser's Fine Foods, Inc.

17 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2024

1) Flex Extenders, 5.2" x 15mm OD x 15mm ID REF S6411P 2) Flex Extender, 5.2" x 15mm OD x 22/15mm ID REF 7 5132 The…

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

Westmed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

Boston Scientific myLUX Patient Application for an Apple Mobile device, Model Number 2939, Version 2.0.101, 2.0.110,…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2024

Horizon Organic Ultra Pasteurized Heavy Whipping Cream, refrigerated, One Pint (473ml), UPC 7 42365 21685 5. There are…

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

Horizon Organic Dairy, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2024

STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP15…

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

Physio-Control, 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.