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.

6901–6925 of 81195

HighFDA (Food)·F-0767-2025·2025-05-21
Bonya Peach Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Peach Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ due to undeclared almonds that may pose a risk to consumers with tree nut allergies.
Product
Bonya Peach 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-1766-2025·2025-05-21
Centurion Sterile Weitlaner Retractor recalled for sterile packaging puncture risk
Medline Industries is recalling Centurion Sterile Weitlaner Retractor 3 x 4 Prong units because the retractors may puncture through the sterile packaging. The product is distributed nationwide.
Product
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0765-2025·2025-05-21
Bonya Blueberry Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Blueberry Yogurt Parfait (8 oz) distributed in NY, PA, MA, and NJ because the product contains undeclared almonds, which poses a risk to consumers with tree nut allergies.
Product
Bonya Blueberry 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-1776-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Body Coil Seal Failure Recall
Philips is recalling 103 Intera 1.5T MRI scanners worldwide because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, or tissue injury to patients.
Product
Intera 1.5T Master/Nova, Model Number: 781106;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0771-2025·2025-05-21
Bonya Coconut Yogurt Parfait Recalled for Undeclared Almonds
Knockroe Inc is recalling Bonya Coconut Yogurt Parfait (8 oz) distributed to NY, PA, MA, and NJ because it contains undeclared almonds, a common allergen.
Product
Bonya Coconut 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-1775-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T Explorer/Nova Dual MRI scanners (Model 781108) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges that could contact patients during scanning and cause skin injuries.
Product
Intera 1.5T Explorer/Nova Dual, Model Number: 781108;
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-1743-2025·2025-05-21
Halyard RAPIDES E-PACK Cardiovascular Procedure Kit Surgical Needle Coating Issue
AVID Medical is recalling Halyard RAPIDES E-PACK Cardiovascular Procedure Convenience Kits due to a raw material defect in surgical needle coating that may cause diminished performance or coating removal during use.
Product
Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V334000·2025-05-21
Volkswagen Atlas rearview camera image can become distorted in reverse
Volkswagen is recalling certain 2024-2025 Atlas and Atlas Cross Sport vehicles because a software error may distort the rearview camera image when the vehicle is in reverse.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1783-2025·2025-05-21
Philips SmartPath to dStream 3.0T MRI Coil Adhesive Failure Recall
Philips is recalling SmartPath to dStream 3.0T MRI systems (Model 782145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
SmartPath to dStream for 3.0T, Model Number: 782145;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V333000·2025-05-21
Mack Recalls 2026 MD Trucks Due to Incorrect Seat Belt Routing
Mack Trucks is recalling 2026 MD vehicles because the center bench seat belt assembly may be routed incorrectly, potentially failing to restrain occupants in a crash.
Product
MACK — MACK MD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1751-2025·2025-05-21
Pruitt Occlusion Catheter Recalled Due to Incomplete Sterile Barrier Seals
LeMaitre Vascular is recalling Pruitt Occlusion Catheters (catalog numbers 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56) because some packages have incomplete sterile barrier seals, potentially compromising product sterility.
Product
Pruitt Occlusion Catheter. Catalog Numbers: 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1749-2025·2025-05-21
Abbott Alinity m Resp-4-Plex AMP Kit Multiplex PCR Test Recall
Abbott Molecular is recalling the Alinity m Resp-4-Plex AMP Kit (List Number 09N79-096) due to reports of increased reactive negative controls and false positive results in respiratory viral testing.
Product
Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the simultaneous qualitative detection and differentiation of RNA from SARS-CoV-2, influenza A virus (flu A), influenza B virus
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-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-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-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
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-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
HighNHTSA·25E036000·2025-05-21
Holley Recalls Fuel Pressure Regulators Due to Leak Risk
Holley Performance Products is recalling specific Fuel Pressure Regulators because a damaged diaphragm may cause a fuel leak, increasing the risk of fire.
Product
FUEL SYSTEM, GASOLINE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1770-2025·2025-05-21
Philips Enterprise 1.5T MRI Equipment Quadrature Body Coil Seal
Philips is recalling Enterprise 1.5T MRI scanners (Model 781145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Enterprise 1.5T, Model Number: 781145;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1742-2025·2025-05-21
Halyard SUTURE PACK CABG Cardiovascular Kit Needle Coating Issue
AVID Medical is recalling Halyard SUTURE PACK CABG Cardiovascular Procedure Convenience Kits due to a raw material defect in the surgical needle coating that may reduce needle performance or cause coating removal during use.
Product
Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1784-2025·2025-05-21
Beckman Coulter DxC 500 AU Chemistry Analyzer Software Calibration Error
Beckman Coulter is recalling the DxC 500 AU Clinical Chemistry Analyzer due to a software error that prevents the analyzer from completing calibration orders under certain conditions, which can delay test result reporting.
Product
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065. The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in samples, in combination with appropriat
Category
Medical Device
Distribution
17 states
ModerateFDA (Drugs)·D-0417-2025·2025-05-21
La Roche-Posay Effaclar Duo Acne Treatment Recalled for Benzene Contamination
La Roche-Posay Effaclar Duo acne treatment is being recalled due to detected trace levels of benzene. The recall affects 2,226,801 units distributed nationwide.
Product
La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, Laboratoire Dermatologique, CAI 86270, La Roche-
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1744-2025·2025-05-21
Contour Gold Eyelid Weight implants recalled for mislabeling
Meddev Corp is recalling Contour Gold Eyelid Weight implants (Model LL3010, 1.0 gm) due to mislabeling. The recall affects 34 units distributed nationwide across 17 states.
Product
Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3010 Product Description: Contour Gold Eyelid Weight, 1.0 gm MedDev Contour and ThinProfile Eyelid Weight Implants are designed for the gravity-assisted treatment of protracted permanent
Category
Medical Device
Distribution
Distributed nationwide