State

Massachusetts product recalls

72,984 recalls have nationwide distribution and so reach Massachusetts. 8,211 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total: 8,211
Critical: 1,171
Severe: 2,013
Most recent: 2026-09-16

Of the 8,211 recalls naming Massachusetts we have scored against our rubric, 1,171 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,013 (25%) are Severe.

Which agencies issued them

These figures cover only the 8,211 recalls whose distribution notice names Massachusetts specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6876–6900 of 81195

SevereFDA (Food)·F-0770-2025·2025-05-21
Bonya Pineapple Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Pineapple Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ because the product contains undeclared almonds, a common allergen that is not listed on the label.
Product
Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-1698-2025·2025-05-21
AirLife Infant Heated Wire Circuit Adapter Disconnection Risk Recall
Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (model AH265) because adapters may disconnect during setup or use, potentially interrupting ventilation to newborns. Disconnection can cause hypoxia, hypercapnia, and organ failure.
Product
Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH265 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit Kit Dual-limb, Dual-heat, high-flow circuit (>4 L/min) Contains AH165 Circuit, AH290 Chamber Compone
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1750-2025·2025-05-21
TufTex Over-the-Wire Embolectomy Catheter incomplete sterile barrier
LeMaitre Vascular is recalling TufTex Over-the-Wire Embolectomy Catheters due to incomplete seals on some packages that compromise the sterile barrier. Affected units were distributed nationwide and internationally.
Product
TufTex Over-the-Wire Embolectomy Catheter. All Catalog numbers: 1651-34, 1651-38, 1651-44, 1651-48, 1651-58, 1651-64, 1651-68, 1651-78, 1651-84, 1651-88, E1651-34, E1651-38, E1651-44, E1651-48, E1651-64, E1651-68, E1651-78, E1651-84, E1651-88, 1651-44J, 1651-48J, 1651-84J, 1
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0420-2025·2025-05-21
Testosterone Cypionate Injection 200 mg/mL Recalled for Sterility Assurance
Empower Pharmacy is recalling Testosterone Cypionate Injection 200 mg/mL (Lot 202364, 8,230 vials) distributed nationwide because the manufacturer cannot assure the product's sterility. Consumers should stop using the product and consult their healthcare provider.
Product
Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only, 5 mL Sterile Multiple-Dose Vial, Compounded by: Empower Pharmacy, 7601 N Sam Houston Pkwy W Ste 100, Houston, TX, 77064, Phone: (877) 562-8577, Compounding Date: 08/20/2024, Beyond Use by Date: 05/28/2025, Lot 202364.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0768-2025·2025-05-21
Bonya Lemon Yogurt Parfait Recalled for Undeclared Almonds
Knockroe Inc is recalling Bonya Lemon Yogurt Parfait (8oz) because it contains undeclared almonds, a common allergen. The product was distributed to New York, Pennsylvania, Massachusetts, and New Jersey.
Product
Bonya Lemon Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-1730-2025·2025-05-21
MedicaLyte Liquid Bicarbonate Concentrate Recalled for Foreign Matter
Nipro Renal Solutions USA is recalling MedicaLyte Liquid Bicarbonate Concentrate (models BC+201 and BC+100) due to the potential presence of visible foreign matter in the product.
Product
MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in corrugated shipper cases (4 bottles per shipper case).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0774-2025·2025-05-21
Bonya Black Cherry Yogurt Parfait Recalled for Undeclared Almonds
Knockroe Inc is recalling Bonya Black Cherry Yogurt Parfait due to undeclared almonds, which pose a risk to people with tree nut allergies. The product was distributed in NY, PA, MA, and NJ.
Product
Bonya Black Cherry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0775-2025·2025-05-21
H&C Farms Raw Premium Tomatoes Recalled for Potential Salmonella
H&C Farms Raw Premium Tomatoes are being recalled due to potential Salmonella contamination. The recall affects tomatoes distributed to eight U.S. states.
Product
H&C Farms Raw Premium Tomatoes, Naturally Grown from Seed Net WT 25 Lbs., 11.34 KG, packaged in cardboard box with lid, multiple packaging sizes of tomatoes: JUMBO PER BOX 38-42 TOMATOES, 5X6 PER BOX 55-62 TOMATOES, 6X6 PER BOX 75-82 TOMATOES, 6X7 PER BOX 85-92 TOMATOES. REFRIGRE
Category
Food
Distribution
8 states
SevereFDA (Food)·F-0776-2025·2025-05-21
Tomatoes Recall Due to Potential Salmonella Contamination
Ray & Mascari, Inc. is recalling tomatoes sold in retail 4-count clam shell containers and bulk cardboard cases due to potential Salmonella contamination. Affected products were distributed in IN, KY, MA, MD, MI, NC, OH, PA, and WI.
Product
Tomatoes, retail 4 Count Vine Ripe Tomatoes packaged in clam shell containers [20 oz. (1 lb. 4 oz) 567g] with UPC# 7 96553 20062 1; 12 retail clam shells per case. Bulk 25# 6x6 tomatoes (cardboard case), bulk 10# 6x6 Tomatoes (cardboard case), bulk 25# Random #2 Tomatoes (cardbo
Category
Food
Distribution
9 states
SevereFDA (Devices)·Z-1727-2025·2025-05-21
iGo2 DC Car Adapter Recall: Overheating and Housing Deformation Risk
Medical Depot Inc. is recalling 89,532 units of the iGo2 DC Car Adapter used with iGo2 Portable Oxygen Concentrator Systems. The DC power supply housing may become excessively hot to the touch and deform, posing a burn and fire hazard.
Product
iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0772-2025·2025-05-21
Bonya Passion Fruit Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Passion Fruit Yogurt Parfait (8 oz) due to undeclared almonds, which poses a risk to consumers with tree nut allergies. The product was distributed to New York, Pennsylvania, Massachusetts, and New Jersey.
Product
Bonya Passion Fruit Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0773-2025·2025-05-21
Bonya Strawberry-Banana Yogurt Parfait Recalled Due to Undeclared Almonds
Knockroe Inc is recalling Bonya Strawberry-Banana Yogurt Parfait (8oz) because the product contains undeclared almonds, which pose a risk to consumers with tree nut allergies.
Product
Bonya Strawberry-Banana Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-1763-2025·2025-05-21
LifeShield Infusion Safety Software Recalled for Drug Library Defects
ICU Medical is recalling LifeShield Drug Library Management software v2.1 and v2.2 due to defects that could allow over-delivery of medication to patients or unauthorized modification of drug parameters.
Product
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1771-2025·2025-05-21
Philips Intera 0.5T Standard MRI System Quadrature Body Coil Seal
Philips is recalling the Intera 0.5T Standard MRI system (Model 781101) because the Quadrature Body Coil seal adhesive may fail and create sharp edges that could injure patients during scanning.
Product
Intera 0.5T Standard, Model Number: 781101;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1782-2025·2025-05-21
Philips SmartPath dStream 1.5T MRI coil may create sharp edges
Philips is recalling SmartPath to dStream 1.5T MRI units (Model 782146) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, lacerations, or tissue injury to patients.
Product
SmartPath to dStream for 1.5T, Model Number: 782146;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1778-2025·2025-05-21
Philips Intera 1.5T MRI Scanner QBC Seal Adhesive Failure Risk
Philips is recalling the Intera 1.5T Power/Pulsar MRI scanner because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Intera 1.5T Power/Pulsar, Model Number: 781105;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V330000·2025-05-21
Ram ProMaster rearview camera image may not display in reverse
Chrysler is recalling certain 2022-2025 Ram ProMaster vehicles because a software error in the security gateway module may prevent the rearview camera image displaying, failing FMVSS 111.
Product
RAM — RAM, BRAUN PROMASTER, RAM PROMASTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1780-2025·2025-05-21
Philips Intera 3.0T Quasar Dual MRI Scanner Coil Seal Adhesive Failure
Philips is recalling the Intera 3.0T Quasar Dual MRI scanner (Model 781150) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Intera 3.0T Quasar Dual, Model Number: 781150;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1772-2025·2025-05-21
Philips Intera 1.0T MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.0T Omni/Stellar MRI systems (37 units: 3 in US, 34 internationally) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that can cause skin injuries during patient scanning.
Product
Intera 1.0T Omni/Stellar, Model Number: 781102;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1777-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Quadrature Body Coil Seal Failure
Philips is recalling the Intera 1.5T Omni/Stellar MRI scanner due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and cause patient injury. The loose seal during scanning could result in skin abrasions, bruises, lacerations, hair loss, or tissue damage.
Product
Intera 1.5T Omni/Stellar, Model Number: 781104;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1781-2025·2025-05-21
Philips Intera CV MRI Quadrature Body Coil Seal Adhesive Failure Recall
Philips is recalling Intera CV MRI units (Model 781107) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning, including skin abrasions, lacerations, or tissue damage.
Product
Intera CV, Model Number: 781107;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1773-2025·2025-05-21
Philips Intera 1.0T MRI Quadrature Body Coil Seal Failure Recall
Philips is recalling Intera 1.0T Power/Pulsar MRI systems (Model 781103) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and injure patients during scanning.
Product
Intera 1.0T Power/Pulsar, Model Number: 781103;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1779-2025·2025-05-21
Philips Intera 1.5T R11 MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T R11 MRI systems because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could contact patients and cause skin injuries.
Product
Intera 1.5T R11, Model Number: 781170;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0769-2025·2025-05-21
Bonya Raspberry Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Raspberry Yogurt Parfait (8oz) because it contains undeclared almonds, which pose an allergy risk. The recall affects 6,984 units distributed to NY, PA, MA, and NJ.
Product
Bonya Raspberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1769-2025·2025-05-21
KliniTray Platte Faxitron Sterile Tissue Resection Examination Board Recalled
KliniTray Platte Faxitron sterile tissue resection margin examination boards (Model 2001155-F) are being recalled due to potential for microbial contamination. Affected units were distributed nationwide.
Product
KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact
Category
Medical Device
Distribution
Distributed nationwide