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.
Reported Nov 12, 2025
Brand Name: Inclusive Product Name: Inclusive Titanium Screw compatible with: Biomet 3i" Certain 3.4/4.1/5.0/6.0 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prismatik Dentalcraft, Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2025
Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion pumps capable of both…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tandem Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2025
Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2025
SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L Prepared with Dipotassium EDTA Purple, Model: 07 6011; SAFE-T-FILL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ASP Global, LLC. dba Anatomy Supply Partners, LLC.
FDA (openFDA device enforcement)
Reported Nov 5, 2025
Brand Name: MEGA Ballast Distal Access Platform Product Name: Mega Ballast Model/Catalog Number: MEGABT09180,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Balt USA, LLC
FDA (openFDA device enforcement)
Reported Nov 5, 2025
CellMek SPS Sample Preparation System, REF: C44603. Software versions 2.2.122.0 and prior, and Instructions for Use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2025
Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code: 07332940000158 Xpert SA Nasal Complete kit; 10 test…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Nov 5, 2025
ChemoLock Bag Spike, 01 units REF: CL-10-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
37 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2025
MIXED NUTS Roasted & Salted NET WT 8 OZ (227g) INGREDIENTS: ALMONDS, WALNUTS, PEANUTS***CASHEWS***HAZELNUTS, BRAZIL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Severn Peanut Company LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 5, 2025
Fusia Asian Inspirations brand Veggie Spring Rolls. Net weight: 10 oz (283.5 g).) retail package identified by UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tai Foong USA Inc.
FDA (openFDA food enforcement)
Reported Oct 29, 2025
Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 29, 2025
Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Southwind Foods LLC dba Great American Seafood Imports Co.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 29, 2025
LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 46MM / XL25/ STER. Product Code: 04.045.346TS. Used in RFN-ADVANCEDTM…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 29, 2025
Floria Dried Apricots, 200 Gram packages, 40 packages per case .
High riskUsing this product could cause serious injury, illness or death — stop using it now.Turkana Food Inc.
FDA (openFDA food enforcement)
Reported Oct 22, 2025
Gluten Free Bean & Rice Burrito. 12 retail units per case. 5.5oz/retail unit. UPC code 042272003525. Frozen.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amy's Kitchen Inc.
FDA (openFDA food enforcement)
Reported Oct 22, 2025
CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
15 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contego Medical LLC
FDA (openFDA device enforcement)
Reported Oct 22, 2025
DuoDERM" Extra Thin dressings are highly flexible, control gel formula dressings designed for use on dry to lightly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Zenith Alpha 2 Thoracic Endovascular Graft, Catalog Prefix ZTA2- Reference Part Numbers ZTA2-P-40-117-W ZTA2-P-40-167…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Medical Incorporated
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used with Disinfection Kit User Manual, REF: UI-185043723
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fisher & Paykel Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported Oct 22, 2025
XERF EFFECTOR 60. Electrosurgical unit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lutronic Corporation
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Brand Name: Branding is not applied to this product. Product Name: DVI display cables Model/Catalog Number: 012-0895-01…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2025
6+ Months SPROUT ORGANICS Made With Organic Sweet Potato, Apple & Spinach NET WT. 3.5 OZ (99g) INGREDIENTS: ORGANIC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sprout Organics Inc.
FDA (openFDA food enforcement)
Reported Oct 15, 2025
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NRT-05055-I The NutraGlide Nasal Feeding…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Technology Inc.
3 more products in this recall
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.