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 Jul 9, 2025
BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2025
Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Peak Cocktails
FDA (openFDA food enforcement)
Reported Jul 9, 2025
BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2025
REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2025
REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2025
Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2025
Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2025
FIREHOOK ARTISAN BAKED CRACKERS CLASSIC SEA SALT NET WT. 8 OZ (227g) INGREDIENTS: ORGANIC WHEAT FLOUR, ORGANIC HONEY,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Firehook
FDA (openFDA food enforcement)
Reported Jul 2, 2025
Spectral CT. Computed tomography X-ray system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Balt USA, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Big Y various sandwiches made to order at deli counter (Subs (small, large, supersub), wrap, panini, grinders); UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Big Y Supermarkets
FDA (openFDA food enforcement)
Reported Jun 25, 2025
5008X HDF Hemodialysis Blood Tubing Set, 24 units per case, with the following models: a. 5008X Standard HDF Bloodline,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Jun 25, 2025
ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001 , and 3) 400021003; infusion pump
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Lancaster LF Authentic Greek Salad Kit, 2/7.125lb. packages, net wt. 14.25lb., Item Code 407079, UPC 13454.38482. This…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc. dba Fresh Creative Foods
FDA (openFDA food enforcement)
Reported Jun 18, 2025
Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Allon 2001. Part Number: 200-00263
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Belmont Instrument LLC
FDA (openFDA device enforcement)
Reported Jun 18, 2025
SCD Comfort Knee Length Small, SKU 84021; Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipman Family Farms
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 18, 2025
Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microtek Medical, Inc.
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Achieva XR Product Numbers: (1) 781153, (2) 781253;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Smartcuts Cucumber Sliced Trays 2/2lb
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sardilli Produce & Dairy Co. Inc.
FDA (openFDA food enforcement)
Reported Jun 18, 2025
3909520 2/5# IMPERIAL FRESH CUCUMBER DICED 3/8 SK-ON ALL LOT CODES 480414 2/5 # IMPERIAL FRESH FC CUCUMBER STRIPED AND…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sysco Corporation
7 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 11, 2025
AMCE GREEK SALAD AUTHENTIC FS, Refrigerated, packaged in clear plastic container, sold by pound, UPC 293070 ##### READY…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Albertsons Companies LLC
FDA (openFDA food 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.