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.

47576–47600 of 82079

ModerateFDA (Devices)·Z-2658-2017·2017-07-12
Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-packaging Error
Encore Medical is recalling 9 units of 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.
Product
3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2665-2017·2017-07-12
Exactech Equinoxe Modular Reverse Pilot-Tip Starter Reamer Recall
Exactech is recalling 928 Equinoxe Modular Reverse Pilot-Tip Starter Reamers to update instructions for use. The update clarifies proper reaming technique to prevent instrument breakage.
Product
EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #: 321-25-01
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2664-2017·2017-07-12
Exactech Equinoxe Glenoid Reamer Recalled for Updated Instructions
Exactech is recalling Equinoxe Glenoid Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38, Catalog #: 321-05-42, and Catalog #: 321-05-46
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2668-2017·2017-07-12
Exactech Equinoxe Reamer Recall Due to Updated Instructions for Use
Exactech is recalling Equinoxe Narrow Modular Reverse Pilot-Tip Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #: 321-45-38, Catalog #: 321-45-42 and Catalog #: 321-45-46
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2663-2017·2017-07-12
Exactech Equinoxe Reverse Starter Reamer Recalled for Updated Instructions
Exactech is recalling 382 Equinoxe Reverse Starter Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01
Category
Medical Device
Distribution
33 states
ModerateFDA (Devices)·Z-2662-2017·2017-07-12
Exactech Recalls Logic Fit Tibial Tamp Heads for Labeling Clarification
Exactech, Inc. is recalling 573 Logic Fit Tibial Tamp Heads to update surgical labeling. The update clarifies proper removal techniques to prevent instrument breakage.
Product
Logic Fit Tibial Tamp Head
Category
Medical Device
Distribution
32 states
ModerateFDA (Drugs)·D-0945-2017·2017-07-12
G & W Clobetasol Propionate Ointment Recalled for Impurity
G & W Laboratories is recalling Clobetasol Propionate Ointment 0.05% due to out-of-specification results for a known impurity.
Product
CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0937-2017·2017-07-12
Methocarbamol USP Recalled for Quality Assurance Deviations
American Pharmaceutical Ingredients LLC is recalling Methocarbamol USP due to lack of quality assurance at the API manufacturer.
Product
Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 g container (NDC: 58597-8023-8). For Prescription Compounding RX Only. Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC 6650 Highland…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2660-2017·2017-07-12
Leica ASP6025 Tissue Processor Recalled for Incorrect Voltage Labeling
Leica Microsystems is recalling 812 ASP6025 Tissue Processors because the voltage labels on the rear alarm connectors are incorrect.
Product
Nussloch GmbH ASP6025 Tissue Processor
Category
Medical Device
Distribution
36 states
ModerateFDA (Food)·F-2423-2017·2017-07-12
Nutri-Dyn Calcium D-Glucarate Plus Recalled Due to Mislabeling
Nutri-Dyn Midwest, Inc. is recalling 856 bottles of Calcium D-Glucarate Plus because they were mistakenly labeled as St. John's Wort during production.
Product
Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9
Category
Food
Distribution
24 states
ModerateFDA (Devices)·Z-2666-2017·2017-07-12
Exactech Equinoxe Modular Reverse Pilot-Tip Reamer Recall for Labeling Clarification
Exactech is recalling Equinoxe Modular Reverse Pilot-Tip Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.
Product
EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer, Catalog #: 321-25-38, Catalog #: 321-25-42 and Catalog #: 321-25-46
Category
Medical Device
Distribution
33 states
ModerateFDA (Drugs)·D-0944-2017·2017-07-12
GSK Recalls Parodontax Toothpaste Due to Possible Metal Presence
GSK Consumer Healthcare is recalling 15,708 tubes of Parodontax Whitening toothpaste due to the possibility of metal in the product.
Product
PARODONTAX — PARODONTAX (STANNOUS FLUORIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0934-2017·2017-07-12
PharMEDium Recalls Ropivacaine HCl Injection Due to Labeling Errors
PharMEDium Services, LLC is recalling 21 pumps of Ropivacaine HCl 0.2% injection due to incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0935-2017·2017-07-12
PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling
PharMEDium Services is recalling two Bupivacaine HCl ON-Q pumps due to incorrect or missing lot and expiration date labeling.
Product
Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 270 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-044-57
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2659-2017·2017-07-12
Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-Packaging
Encore Medical is recalling 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.
Product
3DKNEE(TM) SYSTEM e+, Tibial Insert, RIGHT Sz 8 / 11mm, REF 391-11-708, QTY 01 The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0932-2017·2017-07-12
PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors
PharMEDium Services is recalling 147 Ropivacaine HCl IV pumps nationwide because of incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-25
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0930-2017·2017-07-12
PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Labeling
PharMEDium Services is recalling 79 Ropivacaine HCl IV pumps because of incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-256-09
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0936-2017·2017-07-12
PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling
PharMEDium Services is recalling seven Bupivacaine HCl ON-Q pumps because of incorrect or missing lot and expiration dates.
Product
Bupivacaine HCl 0.25% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-023-09
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0931-2017·2017-07-12
PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors
PharMEDium Services is recalling 22 Ropivacaine HCl pumps nationwide because of incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-03
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0933-2017·2017-07-12
PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Lot and Expiration Dates
PharMEDium Services, LLC is recalling 10 Ropivacaine HCl 0.2% ON-Q pumps nationwide due to incorrect or missing lot and expiration dates.
Product
Ropivacaine HCl 0.2% 750 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 600 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-279-33
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·17V465000·2017-07-11
Kawasaki Recalls 2017 Versys 650 Motorcycles for Loose Tail Light Socket
Kawasaki is recalling 2017 Versys 650 motorcycles because a loose tail/brake light socket may allow the bulb to fall out, increasing crash risk.
Product
KAWASAKI — KAWASAKI VERSYS 650
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17754·2017-07-11
Superpedestrian Recalls Electric Bicycle Conversion Wheels Due to Axle Failure
Superpedestrian is recalling about 230 Copenhagen electric bicycle conversion wheels because the rear axle can fail, posing fall and crash hazards to riders.
Product
Electric bicycle conversion Copenhagen wheels
Category
Consumer Product
Distribution
Distributed nationwide
CriticalNHTSA·17E034000·2017-07-10
Takata Driver Frontal Air Bag Inflator Recall for Rupture Risk
Takata is recalling specific driver-side air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.
Product
AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V435000·2017-07-10
Chrysler Recalls 2011-2014 Vehicles for Alternator Failure Risk
Chrysler is recalling specific 2011-2014 Dodge, Chrysler, and Jeep vehicles because the alternator may fail, causing the vehicle to stall or catch fire.
Product
DODGE — DODGE, CHRYSLER, JEEP DURANGO, 300, CHARGER, CHALLENGER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V437000·2017-07-10
GM Recalls 40,683 Vehicles for Air Bag and Seat Belt Software Defect
General Motors is recalling 40,683 vehicles from 2014-2017 because a software error may prevent front air bags and seat belt pretensioners from deploying in a crash.
Product
CHEVROLET — CHEVROLET, GMC, BUICK CORVETTE, SILVERADO 1500, SIERRA 1500, LACROSSE
Category
Vehicle
Distribution
Distributed nationwide