State

Massachusetts product recalls

72,969 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 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5826–5850 of 81180

CriticalFDA (Devices)·Z-2181-2025·2025-08-20
Manual resuscitators recalled because blocked manometer port may disable pressure gauge
Ambu is recalling 87,156 SPUR II adult resuscitators because the manometer port may be blocked, leaving the manometer non-functional. The FDA classified the action as Class I.
Product
Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Resuscitator w/Mercury Filter, Adult, Catalog Number: 523611051 3 SPUR II Adult Resuscitator, Single Patient Use Resuscitator, Adult, Catalog Number: 523611057 4
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0542-2025·2025-08-20
Sysco foodservice tuna salad recalled over Listeria risk from recalled breadcrumbs
Sysco Imperial Deluxe Tuna Salad in 5 lb foodservice tubs is recalled for potential Listeria monocytogenes contamination traced to recalled Newly Weds Foods breadcrumbs. 70 cases are affected.
Product
Sysco Imperial Deluxe Tuna Salad, Reorder #6526826, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with printed white lid. Keep Refrigerated. Distributed by Sysco Corporation, Houston, TX 77077 UPC on 5lb. TUB: 74865 79721 GTIN on Master Case (2/
Category
Food
Distribution
29 states
CriticalFDA (Devices)·Z-2273-2025·2025-08-20
Carotid stent delivery systems recalled over resistance during withdrawal after deployment
Certain batches of the Carotid WALLSTENT Monorail Endoprosthesis are being removed after complaints of greater than anticipated resistance withdrawing the delivery system. The most serious potential consequence is stroke.
Product
Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent, stent and stent delivery system. Material numbers: H7493915010240 CAROTID WALLSTENT MONORAIL 10.0-24; H7493915010310 CAROTID WALLSTENT MONORAIL 10.0-31; H749391506220 CAROTID WALLSTENT MONORAIL
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0544-2025·2025-08-20
Reser's tuna salad containing pickle relish recalled for Listeria monocytogenes risk
Reser's Tuna Salad in 5 lb foodservice tubs, the version containing pickle relish, is recalled for potential Listeria monocytogenes contamination from recalled breadcrumbs. 108 cases are affected.
Product
Reser's Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in white plastic tub and lid with sticker. Keep Refrigerated. This item contains ingredient Pickle Relish. Distributed by Reser's Fine Foods, Incl, Beaverton, OR. UPC on 5lb. TUB/Lid: 71117 11405 GTIN on Mas
Category
Food
Distribution
29 states
SevereFDA (Devices)·Z-2228-2025·2025-08-20
DreamStation Auto BiPAP units may hold an incorrect device configuration
DreamStation Auto BiPAP non-continuous ventilators are being recalled because the devices may possess a programming error resulting in an incorrect device configuration. 8 units are affected.
Product
DreamStation Auto BiPAP. Non-Continuous Ventilator.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0539-2025·2025-08-20
Signature Cafe tuna salad recalled over Listeria in recalled breadcrumbs
Signature Cafe Premium Tuna Salad, 3 lb foodservice tubs, is being recalled because it contains Newly Weds Foods recalled Japanese style breadcrumbs, with potential Listeria monocytogenes contamination. 165 cases affected.
Product
Signature Cafe Premium Tuna Salad, net wt. 3lb (48oz). Foodservice item to be used by deli. Product is packaged in clear plastic tub with printed white lid. Keep Refrigerated. Distributed by Lucerne Foods, PO Box 99, Pleasanton, CA. UPC on 3lb. TUB: 71117 06036 GTIN on Mast
Category
Food
Distribution
29 states
SevereUSDA FSIS·028-2025·2025-08-20
Sabrositos Hondurenos Recalls Meat Products Produced Without Federal Inspection
Sabrositos Hondurenos, LLC is recalling approximately 32,000 pounds of meat products that were produced without federal inspection and bear false USDA marks.
Product
Sabrositos Hondurenos, LLC, Recalls Various Meat Products Produced Without Benefit of Inspection
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2227-2025·2025-08-20
DreamStation Auto CPAP units may hold an incorrect device configuration
DreamStation Auto CPAP non-continuous ventilators are being recalled because the devices may possess a programming error resulting in an incorrect device configuration. 57 units are affected.
Product
DreamStation Auto CPAP. Non-Continuous Ventilator.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2291-2025·2025-08-20
HeartMate mobile power unit cords may disconnect from a misaligned lock
HeartMate Mobile Power Units are being recalled because misaligned V-Lock features on the power cords prevent the locking mechanism engaging properly and may cause unintended disconnect. 604 units affected.
Product
Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number: 107754 Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device designed to provide
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V532000·2025-08-20
Aston Martin Recalls 2025 Vanquish for Brake Assist Software Defect
Aston Martin is recalling 2025 Vanquish vehicles because a vacuum pump defect may cause loss of power brake assist, increasing stopping distance and crash risk.
Product
ASTON MARTIN — ASTON MARTIN VANQUISH
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-0541-2025·2025-08-20
Reser's gourmet tuna salad recalled over Listeria in recalled breadcrumbs
Reser's Gourmet Tuna Salad, 5 lb foodservice tubs, is being recalled because it contains Newly Weds Foods recalled Japanese style breadcrumbs, with potential Listeria monocytogenes contamination. 240 cases affected.
Product
Reser's Gourmet Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with white lid with white sticker. Keep Refrigerated. Distributed by Reser's Fine Foods, Beaverton, OR. UPC on 5lb. TUB: 71117 85506 GTIN on Master Case (2/5# per case):
Category
Food
Distribution
29 states
SevereNHTSA·25V533000·2025-08-20
Mercedes steering coupling bolt may loosen from the steering rack
Mercedes-Benz is recalling certain 2023-2026 EQE and GLC vehicles because the steering coupling bolt may have been improperly tightened, allowing the coupling to loosen from the steering rack.
Product
MERCEDES-BENZ — MERCEDES-BENZ EQE 500 4MATIC, EQE 350 4MATIC, AMG EQE 53 4MATIC, AMG GLC63 S E
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0465-2025·2025-08-20
La Michoacana variety paletas list cream without declaring milk as source
La Michoacana Minis Variety Paletas 12-count are being recalled because the label includes the ingredient cream but does not include milk as the source. 29,180 units are affected.
Product
La Michoacana Minis Variety Paletas 12-Count 16.5oz UPC: 7-67778-03042-3
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0469-2025·2025-08-20
Helados Mexico variety paletas list cream without declaring milk as source
Helados Mexico Minis Variety Paletas 12-count are being recalled because the label includes the ingredient cream but does not include milk as the source. 42,488 units are affected.
Product
Helados Mexico Minis Variety Paletas 12-Count 18oz UPC:6-82082-61215-1
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0452-2025·2025-08-20
Tikka masala Indian curry sauce recalled over potential metal foreign objects
Sukhi's Tikka Masala Indian Curry Sauce, 3 oz, is recalled for potential contamination with metal pieces. The recall covers 4,869 pounds distributed across more than 25 states.
Product
Sukhi's, TIKKA MASALA INDIAN CURRY SAUCE, NET WT 3 OZ., UPC 7-67226-00163-0, DISTRIBUTED BY: SUKHI'S GOURMET INDIAN FOODS 25823 CLAWITER ROAD, HAYWARD, CA 94545 USA
Category
Food
Distribution
33 states
HighFDA (Drugs)·D-0588-2025·2025-08-20
Carvedilol 25 mg tablets recalled over nitrosamine impurity above FDA limit
Glenmark Carvedilol Tablets USP, 25 mg, in 500-tablet cartons are recalled nationwide after N-Nitroso Carvedilol Impurity-1 was found above the FDA-recommended limit. 14,976 bottles are affected.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0463-2025·2025-08-20
Coconut con crema 6-pack paletas recalled over undeclared milk in cream
La Michoacana Coconut Con Crema 6-Pack Paletas, 16.5 oz, are recalled nationwide because the label lists cream but does not declare milk as its source. 47,065 units are affected.
Product
La Michoacana Coconut Con Crema 6-Pack Paleta 16.5oz UPC: 7-67778-00101-0
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2285-2025·2025-08-20
Knee tibial insert catalog number 341-16-704 recalled for mislabeled size or side
Enovis is recalling 18 EMPOWR 3D Knee tibial inserts, catalog number 341-16-704, lot 148T1057, because the implants carry incorrect size or side labeling.
Product
Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number: 341-16-704 Product Description: Enovis knee devices are intended for treatment of patients who are candidates for knee arthroplasty per the Indication for use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0581-2025·2025-08-20
Metoprolol tartrate tablets recalled for nitrosamine above acceptable daily intake level
Metoprolol Tartrate Tablets USP, 50 mg, distributed by Westminster Pharmaceuticals, are recalled nationwide after N-nitroso-metoprolol was found above the established Acceptable Daily Intake. 16,672 bottles are affected.
Product
Metoprolol Tartrate Tablets, USP, 50 mg, 1000 Tablets, Rx Only, Manufactured by: Renata PLC (General Plant -2), Noyapara, Bhawal Mirzapur, Rajendrapur, Gazipur, 1700 Bangladesh, Distributed by: Westminster Pharmaceuticals, LLC, Nashville, TN 37217, NDC 69367-354-10
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0451-2025·2025-08-20
Classic curry Indian sauce recalled over potential metal pieces in product
Sukhi's Classic Curry Indian Curry Sauce, 3 oz, is recalled for potential contamination with metal pieces. The recall covers 1,125 pounds distributed across more than 25 states.
Product
Sukhi's, CLASSIC CURRY INDIAN CURRY SAUCE, NET WT 3 OZ., UPC 7-67226-00165-4, DISTRIBUTED BY: SUKHI'S GOURMET INDIAN FOODS 25823 CLAWITER ROAD, HAYWARD, CA 94545 USA
Category
Food
Distribution
33 states
HighFDA (Devices)·Z-2283-2025·2025-08-20
Kittner gauze rolls had biological foreign matter and wrong pack quantity
Carefree Surgical Specialties Robotic/Laparoscopy Kittner Rolls Gauze is being recalled for product contamination with biological foreign matter that could compromise sterility, and an incorrect quantity of gauze in sterile packaging.
Product
Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/CS Model/Catalog Number: 15505/25 Product Description: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0579-2025·2025-08-20
Glenmark carvedilol 25 mg tablets exceed the acceptable nitrosamine intake level
Carvedilol Tablets USP 25 mg from Glenmark are being recalled because of the presence of a nitrosamine, N-Nitroso Carvedilol I, above the current Acceptable Intake Level. 4,800 bottles affected.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2278-2025·2025-08-20
FARAWAVE ablation catheters may have cracks in the distal electrode bands
FARAWAVE 1.0 Pulsed Field Ablation Catheters are being recalled because specific manufacturing equipment may have caused cracks in the electrode bands on the catheter's distal end. 445 units affected.
Product
FARAWAVE 1.0 Pulsed Field Ablation Catheter, Product ID M004PF41M401
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0425-2025·2025-08-20
Dessert dip recalled nationwide after plastic foreign material found in product
Park Street Deli Cinnamon Bun Dessert Dip in 7 oz plastic tubs is recalled nationwide for plastic foreign material. 19,368 retail units are affected.
Product
Park Street Deli Cinnamon Bun Dessert Dip Net WT 7oz. in plastic tub UPC 4061462440151
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0578-2025·2025-08-20
Carvedilol 12.5 mg tablets recalled over nitrosamine above acceptable intake level
Glenmark Carvedilol Tablets USP, 12.5 mg, lot 19243202, are recalled nationwide because N-Nitroso Carvedilol I impurity was found above the current Acceptable Intake level. 6,432 bottles are affected.
Product
CARVEDILOL — CARVEDILOL (CARVEDILOL)
Category
Drug
Distribution
Distributed nationwide