State

Massachusetts product recalls

73,722 recalls have nationwide distribution and so reach Massachusetts. 8,248 additional recalls listed Massachusetts specifically in their distribution scope.

What the numbers show

Total: 8,248
Critical: 1,179
Severe: 2,356
Most recent: 2026-10-28

Of the 8,248 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 8,248 recalls whose distribution notice names Massachusetts specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29251–29275 of 81970

ModerateFDA (Drugs)·D-0201-2021·2021-01-13
SCA Pharmaceuticals Recalls Morphine Sulfate Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling 751 syringes of Morphine Sulfate 3 mg/3 mL due to a lack of assurance of sterility and potential defective caps.
Product
Morphine Sulfate 3 mg/3 mL in 0.9% Sodium Chloride (1mg/mL) CII, Rx Only, 3 ml Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004010025
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0795-2021·2021-01-13
Steris Vis-U-All Pouches Recalled for Ink Migration Defect
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may bleed during steam processing.
Product
Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884411
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0787-2021·2021-01-13
Steris Vis-U-All High Temperature Tubing Recalled for Ink Migration
Steris Corporation is recalling Vis-U-All High Temperature Tubing because purple ink on the exterior label may bleed during steam processing, causing cosmetic defects and potential ink transfer to devices.
Product
Vis-U-All High Temperature Tubing 4"x100'. One roll per box; 10 boxes per case 10 rolls/cs Model Number: 881041
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0799-2021·2021-01-13
Steris Vis-U-All Pouches Recalled for Ink Migration on Exterior Labels
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may bleed during steam processing, causing cosmetic defects or ink transfer to devices.
Product
Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884816
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0794-2021·2021-01-13
Steris Vis-U-All Pouches Recalled for Ink Migration
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may migrate during steam processing, causing cosmetic defects and potential ink transfer to devices.
Product
Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box; 4 boxes per case Model Number: 884118
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0797-2021·2021-01-13
Steris Recalls Vis-U-All Pouches Due to Ink Migration Defects
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may bleed during steam processing.
Product
Vis-U-All High Temp 5"x15" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884515
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0791-2021·2021-01-13
Steris Vis-U-All Heat Seal Pouches Recalled for Ink Migration
Steris Corporation is recalling Vis-U-All High Temp Heat Seal Pouches because purple ink on the exterior label may bleed during steam processing.
Product
Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box; 5 boxes per case Model Number: 883610
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0796-2021·2021-01-13
Steris Recalls Vis-U-All Pouches Due to Ink Migration
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may bleed during steam processing.
Product
Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884510
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0798-2021·2021-01-13
Steris Recalls Vis-U-All Pouches Due to Ink Migration Defects
Steris Corporation is recalling Vis-U-All High Temp Self Seal Pouches because purple ink on the exterior label may bleed during steam processing, causing cosmetic defects and potential ink transfer to devices.
Product
Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box; 4 boxes per case Model Number: 884713
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0789-2021·2021-01-13
Steris Recalls Vis-U-All High Temperature Tubing Due to Ink Migration
Steris Corporation is recalling Vis-U-All High Temperature Tubing because purple ink on the exterior label may bleed during steam processing, causing cosmetic defects and potential ink transfer to devices inside the pouch.
Product
Vis-U-All High Temperature Tubing 9"x100'. One roll per box; 10 boxes per case 6 rolls/cs Model Number: 881091
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21E002000·2021-01-12
Hikari LED Headlight Bulbs Recalled for Excessive Glare and Brightness
Ningbo is recalling Hikari LED headlight bulbs sold on Amazon because they create excessive glare for oncoming traffic, increasing crash risk.
Product
EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V005000·2021-01-12
Smeal Recalls 2020 Aerial and Pumper Vehicles for Remote Controller Defect
Smeal is recalling 2020 Aerial and Pumper vehicles because a wireless remote controller defect may cause batteries to discharge faster, potentially hindering firefighting efforts.
Product
SMEAL — SMEAL AERIAL, PUMPER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21E003000·2021-01-12
Strategic Sports Recalls Simpson Shorty OTW Motorcycle Helmets
Strategic Sports is recalling 3,752 Simpson Shorty OTW helmets that lack proper retention and protection, increasing crash injury risk.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·21V004000·2021-01-11
Peterbilt 320 and 520 Trucks Recalled for Steering Column Defect
PACCAR is recalling 2015-2021 Peterbilt 320 and 520 trucks because the steering column support may crack, increasing crash risk.
Product
PETERBILT — PETERBILT 520, 320
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V003000·2021-01-08
Braun Recalls Crestline Ambulances Due to Defective Seat Belt Fasteners
Braun Ambulances is recalling specific Crestline CCL150 ambulances because defective seat belt fasteners may fail, increasing injury risk in a crash.
Product
CRESTLINE COACH — CRESTLINE COACH CCL150 TYPE III, CCL150 TYPE I
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V002000·2021-01-08
Marion Body Works Recalls 2018 Freightliner M2 License Plate Light
Marion Body Works is recalling one 2018 Freightliner M2-106 vehicle because a license plate light may be aimed at other drivers, increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER M2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V001000·2021-01-07
Volvo Recalls 2021 Models for SRS Control Unit Attachment Defect
Volvo is recalling 2021 V60, V90, XC60, and XC90 models because the SRS control unit may detach during a crash, reducing occupant protection.
Product
VOLVO — VOLVO XC90, XC60, V60, V60CC
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21718·2021-01-07
Noble House Recalls Chests and Cabinets Due to Tip-Over Hazards
Noble House Home Furnishings is recalling four models of chests, cabinets, and dressers because they are unstable and can tip over, posing serious hazards to children.
Product
Chests, cabinets and dressers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·21717·2021-01-07
John Deere Recalls Frontier Rotary Tillers Due to Injury Hazard
John Deere is recalling Frontier rotary tillers because some lack a safety sign warning of entanglement hazards. No injuries have been reported.
Product
Frontier model rotary tillers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21E001000·2021-01-07
Automann Recalls Warning Triangle Sets for Reduced Visibility and Stability
Automann is recalling Warning Triangle Sets because their color, reflectivity, and stability may reduce effectiveness, potentially increasing crash risk.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0220-2021·2021-01-06
WishGarden Herbs Recalls Goldenseal Powder Jars Due to Microbial Contamination
WishGarden Herbs is recalling 298 jars of Goldenseal Powder because testing found Cronobacter Sakazakii contamination.
Product
Goldenseal POWDER, 0.25 oz. (7 g) plastic jars, WishGarden Herbs, Inc., Boulder, CO 80301. UPC 6 56490 64137 9
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0218-2021·2021-01-06
Wishgarden Herbs Recalls Happy Ducts Compress Due to Microbial Contamination
Wishgarden Herbs is recalling 46 jars of Happy Ducts Compress because the product tested positive for Cronobacter Sakazakii.
Product
Happy Ducts Compress, 3 oz. plastic jar, www.wishgardenherbs.com, Boulder, CO. 80301. UPC 6 56490 20223 5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0177-2021·2021-01-06
Imprimis Recalls Dexamethasone-Moxifloxacin Injection Due to Sterility Concerns
Imprimis NJOF, LLC is recalling 6,520 vials of Dexamethasone-Moxifloxacin PF Injection because 13 vials were found with faulty crimps, raising concerns about sterility.
Product
Dexamethasone - Moxifloxacin PF Injection (1/5) mg/mL, Imprimis Rx Volume: 1mL/vial, Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B Ledgewood, NJ - 07852 (844)446-6979
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0747-2021·2021-01-06
FDA Recalls Covidien TA Auto Suture Vascular Staplers Due to Damaged Components
The FDA is recalling specific lots of Covidien TA Auto Suture Vascular Staplers because a damaged internal component may prevent adequate hemostasis or cause tissue damage.
Product
Covidien TA Auto Suture Vascular Stapler with DST Series Technology 30mm-V 3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3S
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0766-2021·2021-01-06
BD Phoenix PMIC-110 Recalled for False SXT Resistance Results
Becton Dickinson & Co. is recalling BD Phoenix PMIC-110 IVDs due to false resistant SXT results with S. aureus, which could impact antibiotic treatment.
Product
BD Phoenix PMIC-110: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 449036:
Category
Medical Device
Distribution
Distributed nationwide