State

Massachusetts product recalls

73,596 recalls have nationwide distribution and so reach Massachusetts. 8,242 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total: 8,242
Critical: 1,179
Severe: 2,356
Most recent: 2026-10-21

Of the 8,242 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 2,356 (29%) are Severe.

Which agencies issued them

These figures cover only the 8,242 recalls whose distribution notice names Massachusetts specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

726–750 of 81838

CriticalFDA (Drugs)·D-0851-2026·2026-09-09
Optimal Balance Pharmacy Recalls Contaminated Glutathione Injection Vials
Optimal Balance Pharmacy is recalling 53 vials of Glutathione 200 mg/mL due to bacterial endotoxin contamination.
Product
Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only, RX only, Optimal Balance Pharmacy, 2204 Cypress Creek Pkwy Suite F, Houston, TX 77090
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3086-2026·2026-09-09
Fresenius 5008X HD/HDF Blood Tubing Set Recalled for Leak Risk
Fresenius Medical Care is recalling 18,600 units of 5008X HD/HDF blood tubing sets due to a heightened probability of blood leaks that could cause blood loss and hypovolemia.
Product
5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0819-2026·2026-09-09
Baxter Recalls Vasopressin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Vasopressin in 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
VASOPRESSIN IN 0.9% SODIUM CHLORIDE — VASOPRESSIN IN 0.9% SODIUM CHLORIDE (VASOPRESSIN IN 0.9% SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1309-2026·2026-09-09
Hampton Grocer Lactation Granola Recalled for Salmonella Contamination Risk
The Hampton Grocer is recalling Small Batch Lactation Granola due to potential Salmonella contamination. Consumers should stop eating the product and return it for a refund.
Product
THE HAMPTON GROCER brand; Lacnola; SMALL BATCH LACTATION GRANOLA, 8oz, stand up pouches; NUTRIENT DENSE INGREDIENTS + MORINGA; SUPPORTS + PROMOTES HEALTHY LACTATION; INGREDIENTS Organic Gluten Free Oats Organic Maple Syrup Organic Pumpkin Seeds Organic Coconut Oil Almond Butter…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3085-2026·2026-09-09
Fresenius 5008X Blood Tubing Set Recalled for Potential Blood Leak
Fresenius Medical Care is recalling 5008X HD/HDF Standard Blood Tubing Sets due to a heightened probability of blood leak from the Arterial Alpha Clip connection.
Product
5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3061-2026·2026-09-09
Medline Eye and Cataract Kits Recalled for Potential Sterility Breach
Medline is recalling 2,080 eye and cataract preop kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) EYE KIT, Model Number: DYKM2751; 2) EYE KIT, Model Number: DYKM2751A; 3) CATARACT PREOP KIT, Model Number: DYKS1583A; 4) CATARACT PREOP KIT, Model Number: DYKS1583B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3063-2026·2026-09-09
Medline Blood Draw and Phlebotomy Kits Recalled for Sterility Breach
Medline is recalling approximately 996,692 blood draw and phlebotomy kits due to potential sterility breaches in the packaging. The defect may expose patients to microbial contamination.
Product
Medline Convenience Kits: 1) BLOOD DRAW KIT, Catalog Number: DYLAB1081; 2) WHOLE BLOOD PHLEBOTOMY KIT, Catalog Number: DYNDB3005D; 3) QP KIT, Catalog Number: DYNDB3005F; 4) DOUBLE RED CELL PHLEBOTOMY KIT, Catalog Number: DYNDB3006C; 5) PLATELET PHLEBOTOMY KIT, Catalog…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V576000·2026-09-09
Ford Recalls 2026 F-150s Due to Rear Axle Bearing Defect
Ford is recalling 2026 F-150 vehicles because incorrect rear axle tail bearings may cause wheel lock-up or driveshaft separation, increasing crash risk.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0809-2026·2026-09-09
Baxter Recalls Famotidine Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Famotidine Injection due to CGMP deviations. The product was distributed in the US, Puerto Rico, and Chile.
Product
FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0810-2026·2026-09-09
Baxter Recalls Dexmedetomidine Hydrochloride Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Dexmedetomidine Hydrochloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Galaxy 100 mL Single Dose Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-9557-12.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0821-2026·2026-09-09
Baxter Recalls Daptomycin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Daptomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall covers the US, Puerto Rico, and Chile.
Product
Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0718-12.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3084-2026·2026-09-09
Fresenius Medical Care Recalls 5008X Standard HD Pre-Flush Blood Tubing Sets
Fresenius Medical Care is recalling 120 units of 5008X Standard HD Pre-Flush Blood Tubing Sets due to a heightened probability of blood leaks during treatment.
Product
5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3062-2026·2026-09-09
Medline Convenience Kits Recalled for Potential Sterility Breach
Medline is recalling 18,290 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) ORTHO ASPIRATION KIT, Model Number: DYKM1636A; 2) SHOULD BLOCK KIT, Model Number: DYKM1881A; 3) TRIMA KIT, Model Number: DYNDB3077C
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26E063000·2026-09-09
Ford Recalls Battery Energy Control Modules for Software Defect
Ford is recalling specific Battery Energy Control Modules (BECM) because software errors may cause incorrect charge readings or overheating, increasing crash and fire risks.
Product
ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY:MANAGEMENT SYSTEM/ENERGY CONTROL MODULE (BMS/BECM):SOFTWARE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3048-2026·2026-09-09
Medline Convenience Kits Recalled for Potential Sterility Breach
Medline is recalling 104 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT, Model Number: ACC010741; 2) KIT ANESTHESIA L&D A- LINE SET, Model Number: DYKMBNDL199A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3057-2026·2026-09-09
Medline Blood Culture Kits Recalled for Potential Sterility Breach
Medline is recalling 3,650 blood culture kits nationwide due to potential packaging defects that may compromise sterility and expose patients to microbial contamination.
Product
Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC, Model Number: DYNDH1193; 2) BLOOD CULTURE KIT 2 W/CONNECT, Model Number: DYNDH1487A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0817-2026·2026-09-09
Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to CGMP deviations. The affected product was distributed in the US, Puerto Rico, and Chile.
Product
CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V583000·2026-09-09
Daimler Trucks Recalls Freightliner and Western Star Trucks for Brake Defect
Daimler Trucks North America is recalling certain 2020-2023 Freightliner Cascadia and 2022 Western Star 49X trucks because corroded brake valves may cause the vehicle to pull during braking.
Product
FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 49X
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·021-2026·2026-09-09
El Eden Recalls Ineligible Pork Crackling Potato Chips from Colombia
El Eden Import Distributor Corp. is recalling potato chips containing pork cracklings imported from Colombia because the country is ineligible to export meat to the U.S.
Product
El Eden Import Distributor Corp Recalls Ineligible Pork Cracklings Products Imported from The Republic of Colombia
Category
Food
Distribution
6 states
SevereFDA (Drugs)·D-0820-2026·2026-09-09
Baxter Recalls Vancomycin Injection Due to CGMP Deviations
Baxter Healthcare is voluntarily recalling specific lots of Vancomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3060-2026·2026-09-09
Medline C-Section Prep Kits Recalled for Potential Sterility Breach
Medline is recalling 352 C-Section Prep kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) C-SECTION PREP, Model Number: DYNJ32702B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0814-2026·2026-09-09
Baxter Recalls Nexterone Amiodarone Injection Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Nexterone (amiodarone hydrochloride) injection due to Current Good Manufacturing Practice (CGMP) deviations.
Product
NEXTERONE — NEXTERONE (AMIODARONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V578000·2026-09-09
Ford Recalls 2023-2027 F-150 Trucks for Fuel Tank Securing Defect
Ford is recalling 2023-2027 F-150 vehicles because the fuel tank may be improperly secured, posing risks of fuel leaks, engine stalls, or the tank detaching while driving.
Product
FORD — FORD F-150
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0847-2026·2026-09-09
Golden State Medical Supply Recalls Prasugrel Tablets for Failed Dissolution
Golden State Medical Supply is recalling 6,791 bottles of 10mg Prasugrel tablets because the product failed dissolution specifications.
Product
PRASUGREL — PRASUGREL (PRASUGREL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3053-2026·2026-09-09
Medline Ultrasound Breast Pack Recalled for Potential Sterility Breach
Medline is recalling 300 Ultrasound Breast Packs due to packaging defects that may compromise sterility, posing a risk of microbial contamination.
Product
Medline Convenience Kits: 1) ULTRASOUND BREAST PACK, Model Number: DYNJ63375C
Category
Medical Device
Distribution
Distributed nationwide