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 48,122 notices were distributed nationwide, so they reach Massachusetts too — those are in the archive.
Reported Jun 28, 2017
Proteus 235
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Creganna Medical Devices
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2017
AAHU BARAH, DRY FIG, NET WT. 1 LB, PRODUCT OF PAKISTAN
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Global Commodities Inc.
FDA (openFDA food enforcement)
Reported Jun 21, 2017
Philips DigitalDiagnost 3.1.x X-Ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Acetaminophen 325mg tablets, 120-count bottles, Pk By Safecor Health Woburn, MA 01801, NDC 00904198280.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Safecor Health, LLC
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 21, 2017
Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Jun 14, 2017
California Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar; Ingredients (incorrect) Garlic, Canola…
High riskUsing this product could cause serious injury, illness or death — stop using it now.California Sun Dry Foods
FDA (openFDA food enforcement)
Reported Jun 14, 2017
DePuy Synthes various orthopedic instruments modified by U.S. Distributors These instruments are used in various…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Jun 14, 2017
Golden Platter Foods Inc. Recalls Poultry and Beef Products
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Platter Foods Inc.
USDA FSIS
Reported Jun 14, 2017
KRISPPE CLAM-FRY-MIX NET WEIGHT 5 lbs., 25 lbs., 50 lbs.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Krisppee Products Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 14, 2017
STILL RIDING FOODS GLUTEN FREE PIZZA CRUST; Sold in the following package sizes: 36/9" NET WT 15lbs (6.80kg); 12/12"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Still Riding Foods, LLC
FDA (openFDA food enforcement)
Reported Jun 9, 2017
Pork King Sausage, Inc. Recalls Raw Sausage Link Products Due to Misbranding and Undeclared Allergen
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pork King Sausage, Inc.
USDA FSIS
Reported Jun 8, 2017
Aldon Food Corp. Recalls Chicken Salad Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Aldon Food Corporation
USDA FSIS
Reported Jun 8, 2017
Water Lilies Food Inc., Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Water Lilies Food, LLC
USDA FSIS
Reported Jun 7, 2017
The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Scale Mfg Co.
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Adenovirus (20/11 & 2/6); 0.5 mL Catalog # 212M-15; and 7.0 mL Catalog number 212M-18 Microbiology - Analyte Specific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cell Marque Corporation
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Kite Hill Mushroom and Ricotta Ravioli; frozen Ravioli made with almond milk ricotta: 9 oz. package. UPC 856624004173…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lyrical Foods Inc.
FDA (openFDA food enforcement)
Reported Jun 7, 2017
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jun 7, 2017
AIA-PACK TPOAb CONTROL SET
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tosoh Bioscience, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Trident Item # 421048, Multi-Grain Alaskan Cod, Frozen, RETAIL packages, Net wt. 12 oz. UPC 0 28029 21048 4 The retail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trident Seafoods Corp. - Island Enterprise M/V
7 more products in this recall
FDA (openFDA food enforcement)
Reported May 31, 2017
Ceftriaxone TX 32 US S30, Ref 412302 and Ceftriaxone TX 32 US F100, Ref 507058 ETEST is a quantitative technique for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
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.