State

Massachusetts product recalls

73,827 recalls have nationwide distribution and so reach Massachusetts. 8,252 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total: 8,252
Critical: 1,179
Severe: 2,360
Most recent: 2026-11-04

Of the 8,252 recalls naming Massachusetts we have scored against our rubric, 1,179 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,360 (29%) are Severe.

Which agencies issued them

These figures cover only the 8,252 recalls whose distribution notice names Massachusetts specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48151–48175 of 82079

LowFDA (Devices)·Z-2252-2017·2017-06-14
Argon Medical Recalls Arterial Access Needles Due to Packaging Defect
Argon Medical Devices is recalling specific arterial access needles due to a potential packaging defect involving unsealed pouches.
Product
Clear Flashback Needle 7cm x 18G AMC/4; Clear Flashback Needle 2.5 cm x 21G AMC/4; Winged Arterial Needle 7cm x 18G AMC/4; Clear Flashback Needle 7 cm x 19G AMC/4 Usage: Argon Arterial Access Needles are designed to provide vascular access for the percutaneous introduction…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2316-2017·2017-06-14
MedTest DX Assayed Human Multi Sera Control Recall for Out-of-Spec Values
Medtest Holdings, Inc. is recalling MedTest DX Assayed Human Multi Sera Control Level 1 and Level 2 because control values are outside of specification.
Product
MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2 (HEC200) HEC200 " Sml amber glass vial with rubber stopper and black plastic screw cap. " 1 0 control vials per box, 12 cell foam insert. HNC200 " Sml amber glass vials with rubber stopper and green…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0897-2017·2017-06-14
Hetero USA Recalls Acyclovir Tablets Due to Human Hair Presence
Hetero USA Inc. is recalling 13,692 bottles of Acyclovir 800 mg tablets because human hair was found melded into the tablets.
Product
ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·070-2017·2017-06-13
OFD Foods Recalls Beef Hash Due to Possible Rubber Contamination
OFD Foods is recalling Mountain House freeze-dried beef hash due to possible rubber contamination. No illnesses have been reported.
Product
OFD Foods LLC — OFD Food, LLC. Recalls Beef Products Due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·17V376000·2017-06-13
Dodge Grand Caravan Recalled for Air Bag Wiring Defect
Chrysler is recalling 2011-2012 Dodge Grand Caravan vehicles because the driver's air bag wiring may chafe and short circuit, causing unexpected deployment.
Product
DODGE — DODGE GRAND CARAVAN
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17176·2017-06-13
Trango Recalls Vergo Belay Devices Due to Fall and Injury Hazards
Trango is recalling about 2,600 Vergo belay devices because the handle can loosen, causing the braking system to malfunction and posing fall hazards to climbers.
Product
Vergo belay devices (climbing tool)
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17177·2017-06-13
Noble House Recalls Dining Chairs Due to Leg Breakage and Fall Hazard
Noble House is recalling about 3,300 dining chairs because the legs can break, posing a fall hazard. Consumers should stop using the chairs and contact the company for a free repair kit.
Product
Dining chairs
Category
Consumer Product
Distribution
Distributed nationwide
ModerateNHTSA·17V375000·2017-06-13
Chrysler Recalls 2017 Pacifica Plug-in Hybrid for Incorrect Tire Placard Labeling
Chrysler is recalling 2017 Pacifica Plug-in Hybrid vehicles because the tire placard incorrectly lists seating capacity and weight limits, potentially causing vehicle overloading.
Product
CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·065-2017·2017-06-09
Conagra Recalls Spaghetti and Meatball Products for Undeclared Milk Allergen
Conagra Brands is recalling approximately 717,338 pounds of spaghetti and meatball products because they contain undeclared milk, a known allergen.
Product
Hometown Food Company — Conagra Brands, Inc. Recalls Spaghetti and Meatball Products Due To Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereUSDA FSIS·067-2017·2017-06-09
Tyson Recalls Breaded Chicken Products Due to Undeclared Milk Allergen
Tyson Foods is recalling approximately 2.5 million pounds of ready-to-eat breaded chicken products because they may contain undeclared milk, a known allergen.
Product
Tyson Foods, Inc. — Tyson Foods Inc. Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereUSDA FSIS·068-2017·2017-06-09
Gourmet Boutique Recalls Breaded Chicken Products Due to Undeclared Milk Allergen
Gourmet Boutique LLC is recalling approximately 294,744 pounds of ready-to-eat breaded chicken products because they may contain undeclared milk, a known allergen.
Product
Gourmet Boutique, LLC — Gourmet Boutique LLC Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereUSDA FSIS·064-2017·2017-06-09
Pork King Sausage Recalls Raw Sausage Links for Undeclared Milk Allergen
Pork King Sausage, Inc. is recalling approximately 44,035 pounds of raw sausage link products because they may contain undeclared milk, a known allergen.
Product
Pork King Sausage, Inc. — Pork King Sausage, Inc. Recalls Raw Sausage Link Products Due to Misbranding and Undeclared Allergen
Category
Food
Distribution
13 states
HighNHTSA·17V371000·2017-06-09
Chrysler Recalls 2017 Pacifica Plug-In Hybrids for Inverter Defect
Chrysler is recalling 2017 Pacifica Plug-In Hybrids because a power inverter defect may cause the vehicle to stop moving, increasing crash risk.
Product
CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·062-2017·2017-06-08
Aldon Food Recalls Chicken Salad Due to Undeclared Milk Allergen
Aldon Food Corporation is recalling approximately 18,570 pounds of chicken salad products because they contain undeclared milk, a known allergen.
Product
Aldon Food Corporation — Aldon Food Corp. Recalls Chicken Salad Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
9 states
SevereUSDA FSIS·063-2017·2017-06-08
Water Lilies Recalls Breaded Chicken for Undeclared Milk Allergen
Water Lilies Food Inc. is recalling approximately 4,335 pounds of ready-to-eat breaded chicken products because they may contain undeclared milk, a known allergen.
Product
Water Lilies Food, LLC — Water Lilies Food Inc., Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
10 states
SevereUSDA FSIS·061-2017·2017-06-08
Maid-Rite Recalls Beef Products Due to Undeclared Milk Allergen
Maid-Rite Specialty Foods is recalling approximately 174,000 pounds of beef products because they contain undeclared milk, a known allergen.
Product
Maid-Rite Specialty Foods, Inc — Maid-Rite Specialty Foods, LLC. Recalls Beef Products Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
HighNHTSA·17V370000·2017-06-08
Volvo Recalls 2017 XC90 Vehicles for Seat Belt Component Defect
Volvo is recalling 2017 XC90 vehicles because a seat belt component may detach and become a projectile, increasing injury risk.
Product
VOLVO — VOLVO XC90
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V369000·2017-06-08
Supreme Signature Van and Kold King Recall for Rear Reflector Height
Supreme is recalling 2007-2017 Signature Van and Kold King vehicles because rear reflex reflectors may be mounted too high, failing federal safety standards and increasing crash risk.
Product
SUPREME — SUPREME SIGNATURE VAN, KOLD KING
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17175·2017-06-08
GT Mountain Bicycles Recalled Due to Handlebar Crack Hazard
Cycling Sports Group is recalling about 1,000 GT mountain bicycles because the handlebars can crack, posing a fall hazard to consumers.
Product
GT mountain bicycles
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17V368000·2017-06-07
Porsche Recalls Panamera and Cayenne Models for Engine Stall Risk
Porsche is recalling specific 2010-2012 Panamera and 2011 Cayenne vehicles because loose camshaft controllers may cause the engine to stall, increasing crash risk.
Product
PORSCHE — PORSCHE PANAMERA S, PANAMERA 4S, PANAMERA TURBO, PANAMERA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0877-2017·2017-06-07
SCA Pharmaceuticals Recalls Cefazolin Sodium Bags Due to Leaking
SCA Pharmaceuticals is recalling 70 bags of cefazolin sodium due to leaks at the seam, which compromises the product's sterility.
Product
ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 3g, Total Approximate Volume 115 mL, Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0524-32
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0879-2017·2017-06-07
SCA Pharmaceuticals Recalls Phenylephrine Injectable Bags Due to Leaking
SCA Pharmaceuticals is recalling 30 bags of Phenylephrine HCL injectable solution because the bags are leaking at the seam, compromising sterility.
Product
PHENYLephrine HCL in 0.9% Sodium Chloride injectable, 10 mg (Final Concentration = 0.1 mg per mL) Total Volume 100 mL, Single Dose Container bag, Preservative Free (Contains Sulfites), Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC: 70004-0810-32
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0871-2017·2017-06-07
SCA Pharmaceuticals Recalls Morphine Sulfate Injectable Bags Due to Leaking
SCA Pharmaceuticals is recalling 56 bags of morphine sulfate in 0.9% Sodium Chloride injectable because the bags are leaking at the seam, compromising sterility.
Product
morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100 mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-55
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0870-2017·2017-06-07
SCA Pharmaceuticals Recalls Morphine Sulfate Injectable Bags Due to Leaking
SCA Pharmaceuticals is recalling 80 bags of morphine sulfate injectable solution because the bags are leaking at the seam, compromising sterility.
Product
morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-32.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0874-2017·2017-06-07
SCA Pharmaceuticals Recalls Fentanyl Injectable Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling fentanyl citrate injectable bags because they are leaking at the seam, which compromises sterility.
Product
fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable,20 mcg per mL, Single Dose Container bag, (Total fentanyl Dose 2,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-203-32
Category
Drug
Distribution
Distributed nationwide