State

Massachusetts product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43051–43075 of 82069

CriticalFDA (Food)·F-1423-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Products Due to Salmonella Risk
Triangle Pharmanaturals LLC is recalling Molecule Kratom White Borneo products in various formats due to potential Salmonella contamination.
Product
Molecule Kratom White Borneo in 20 capsule, 80 capsule, 45 gram powder, and 250 gram powder plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
CriticalFDA (Food)·F-1415-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Products Due to Salmonella Risk
Triangle Pharmanaturals LLC is recalling all Kratom products due to potential Salmonella contamination. The recall covers Raw Form Organics Maeng Da Kratom Ruby Red capsules.
Product
Raw Form Organics Maeng Da Kratom Ruby Red; R150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
CriticalFDA (Food)·F-1438-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Capsules Due to Salmonella Contamination Risk
Triangle Pharmanaturals LLC is recalling Third Eye Kratom Bali capsules because all Kratom products from the firm may be contaminated with Salmonella.
Product
Third Eye Kratom Bali in 300 capsule plastic bottles. Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
CriticalFDA (Food)·F-1434-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Capsules Due to Salmonella Risk
Triangle Pharmanaturals LLC is recalling Live Well Kratom Green Maeng Da capsules in 150 and 300-count bottles due to potential Salmonella contamination.
Product
Live Well Kratom Green Maeng Da in 150 capsule and 300 capsule plastic bottles. Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
CriticalFDA (Food)·F-1419-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Products Due to Salmonella Risk
Triangle Pharmanaturals LLC is recalling Molecule Kratom Super Green Malay products because they may be contaminated with Salmonella.
Product
Molecule Kratom Super Green Malay in 20 capsule, 80 capsule, 45 gram, and 250 gram plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
SevereNHTSA·18V322000·2018-05-16
McNeilus Recalls 2008-2018 Bridgemaster V Mixers Due to Tank Rupture Risk
McNeilus is recalling 2008-2018 Bridgemaster V concrete mixers because a hydraulic tank may overpressurize and rupture, posing risks of injury and road hazards.
Product
MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1578-2018·2018-05-16
Vyaire Medical Recalls AirLife Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 20 AirLife Resuscitation Broselow Hinkle Kits because the mask component may stick, making it difficult to disconnect from the device.
Product
AirLife Resuscitation, Broselow Hinkle Kit Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1580-2018·2018-05-16
Vyaire Medical Recalls AirLife Infant Resuscitators Due to Mask Sticking
Vyaire Medical is recalling 198 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Product
AirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, manometer, PEEP valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1548-2018·2018-05-16
Vyaire Medical Recalls AirLife Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 24 AirLife Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Adult, with mask, oxygen reservoir bag, CO2 detector Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1549-2018·2018-05-16
Vyaire Medical Recalls AirLife Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 18 AirLife Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Adult, with mask, oxygen reservoir bag, CO2 detector, manometer Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1561-2018·2018-05-16
Vyaire Medical Recalls AirLife Infant Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 6 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Infant, with mask, 40 inch oxygen reservoir tubing, pressure-relief valve, CO2 detector, manometer Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1581-2018·2018-05-16
Vyaire Medical Recalls AirLife Infant Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 180 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Infant, with mask, oxygen reservoir bag, pressure-relief valve, PEEP valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1554-2018·2018-05-16
Vyaire Medical Recalls Pediatric AirLife Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 8,058 pediatric AirLife resuscitation devices because the mask may stick to the elbow, making it difficult or impossible to disconnect.
Product
AirLife Resuscitation, Pediatric, with mask, 40inch oxygen reservoir tubing, pressure-relief valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1556-2018·2018-05-16
Vyaire Medical Recalls AirLife Infant Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling 180 AirLife Infant Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, manometer Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1483-2018·2018-05-16
Draeger Fabius Tiro Anesthesia Machines Recalled for Ventilation Failure Risk
Draeger Medical is recalling 26 Fabius Tiro anesthesia machines because automatic ventilation may fail if motor position detection is disturbed.
Product
Fabius Tiro, anesthesia machine, catalog no. 8606000 Product Usage: The products are inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1391-2018·2018-05-16
Labrada Nutrition Recalls Lean Pro 8 Vanilla Protein Powder for Undeclared Egg
Labrada Nutrition is recalling specific lots of Lean Pro 8 Vanilla protein powder due to undeclared egg, a major food allergen.
Product
Lean Pro 8 Vanilla 2,268g (5lb) Tub
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1426-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Capsules Due to Salmonella Risk
Triangle Pharmanaturals LLC is recalling Naturally Kratom White Maeng Da capsules due to potential Salmonella contamination.
Product
Naturally Kratom White Maeng Da in 6 capsule bags. Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
SevereFDA (Devices)·Z-1568-2018·2018-05-16
Vyaire Medical Recalls AirLife Resuscitation Devices Due to Mask Sticking
Vyaire Medical is recalling AirLife Resuscitation devices because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Adult, with mask, oxygen reservoir bag, PEEP valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1435-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Capsules Due to Salmonella Risk
Triangle Pharmanaturals LLC is recalling Live Well Kratom Red Maeng Da capsules in 150 and 300-count bottles due to potential Salmonella contamination.
Product
Live Well Kratom Red Maeng Da in 150 capsule and 300 capsule plastic bottles. Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
SevereFDA (Food)·F-1414-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Capsules Due to Salmonella Risk
Triangle Pharmanaturals LLC is recalling Raw Form Organics Maeng Da Kratom Ivory White capsules because they may be contaminated with Salmonella.
Product
Raw Form Organics Maeng Da Kratom Ivory White; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
SevereFDA (Devices)·Z-1566-2018·2018-05-16
Vyaire Medical Recalls AirLife Infant Resuscitators Due to Mask Sticking
Vyaire Medical is recalling 3,600 AirLife Infant Resuscitators because the mask may stick to the elbow, making it difficult to disconnect.
Product
AirLife Resuscitation, Infant, with mask, oxygen reservoir bag, pressure-relief valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1484-2018·2018-05-16
Draeger Fabius Tiro M Anesthesia Machine Recalled for Ventilator Failure Risk
Draeger Medical is recalling one Fabius Tiro M anesthesia machine because automatic ventilation may fail if motor position detection is disturbed.
Product
Fabius Tiro M, anesthesia machine, catalog no. 8608400 Product Usage: The products are inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1431-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Products Due to Salmonella Contamination Risk
Triangle Pharmanaturals LLC is recalling Lifted Kratom Red Maeng Da products due to potential Salmonella contamination. The recall covers powder and capsule bottles distributed across multiple states.
Product
Lifted Kratom Red Maeng Da in 45 gram powder, 150 capsule and 300 capsule plastic bottles.. Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
SevereFDA (Food)·F-1433-2018·2018-05-16
Triangle Pharmanaturals Recalls Kratom Products Due to Salmonella Contamination Risk
Triangle Pharmanaturals LLC is recalling Lifted Kratom Gold Bali products because they may be contaminated with Salmonella.
Product
Lifted Kratom Gold Bali in 45 gram powder, 150 capsule and 300 capsule plastic bottles. Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
Category
Food
Distribution
23 states
SevereFDA (Food)·F-1401-2018·2018-05-16
FDA Recalls Energique Herbal Supplements for Unapproved Drug Claims
Grato Holdings is recalling Energique herbal supplements because they are marketed as unapproved new drugs based on disease claims.
Product
Energique, Herbal Supplement, Octocom,; Dist. by Energique, Inc. Woodbine, IA 51579
Category
Drug
Distribution
Distributed nationwide