State

Massachusetts product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36001–36025 of 81989

HighFDA (Devices)·Z-2294-2019·2019-08-28
TiSport Recalls TiLite Wheelchair Anti-Tip Tubes for Tipping Risk
TiSport is recalling 1,452 TiLite wheelchairs because the anti-tip tubes may fail, allowing the chair to tip backwards.
Product
TiLite X-Short anti-tip tubes, models TRA, AERO T, ZRA, AERO Z, 2GX, AERO X, Twist, and AERO R, a component of the TiLite wheelchair (anti-tip extension for manual wheelchairs). Product Usage: The affected component is part of a manual wheelchair to provide mobility to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2071-2019·2019-08-28
Elevation Foods Recalls Fresket Egg Salad Due to Listeria Monocytogenes
Elevation Foods is recalling Fresket egg salad because Listeria monocytogenes was found in the product. The recall covers specific cases distributed to multiple states.
Product
Fresket egg salad packaged in 32oz plastic cup with lid, 2 cups per case, refrigerated
Category
Food
Distribution
9 states
HighFDA (Devices)·Z-2290-2019·2019-08-28
Siemens IMMULITE 2000 Progesterone Test Recalled for Potential Low Results
Siemens is recalling IMMULITE 2000 Progesterone tests because some samples may produce falsely low results, potentially leading to unnecessary medication.
Product
IMMULITE 2000 Progesterone; Models US: L2KPW2, L2KPW6 and OUS: L2KPW2(D), L2KPW6(D); SMN Numbers US: 10901873, 10901874 and OUS 10381181, 10381170
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2296-2019·2019-08-28
BD Vacutainer Tubes Recalled for False Carboxyhemoglobin Results
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Product
BD Vacutainer Lithium HeparinN (LH) 37 USP Units Blood Collection Tubes, Catalog Number 366664
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2061-2019·2019-08-28
Green Water Recalls Multiple Herbal Tinctures and Teas Due to Salmonella Risk
Green Water, LLC is recalling several herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Product
Taspen s Organics, Breathe Easy Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2343-2019·2019-08-28
Siemens MAGNETOM Skyra MRI Devices Recalled for Quench Venting System Defect
Siemens is recalling 44 MAGNETOM Skyra MRI devices due to a potential open port in the quench venting system when using an optional horizontal outlet.
Product
MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-2319-2019·2019-08-28
Qiagen QIAsymphony SP Software 5.0.3 Recalled for Barcode Assignment Error
Qiagen is recalling QIAsymphony SP software version 5.0.3 because it incorrectly assigns 2D barcode eluate IDs to samples, which could lead to incorrect patient reporting.
Product
QIAsymphony SP SOW 5.0.3, software used with the QIAsymphony SP Instrument (The QIAsymphony SP instrument is designed to perform automated purification of nucleic acids-IVD) Model Number: 9001297 Product Usage: The QIAsymphony SP instrument is designed to perform automated…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2289-2019·2019-08-28
Siemens IMMULITE 1000 Progesterone Test Recall for Low Results
Siemens is recalling IMMULITE 1000 Progesterone tests because they may produce falsely low results, potentially leading to unnecessary progesterone supplementation.
Product
IMMULITE 1000 Progesterone, Model LKPW1, SMN Number 10381128
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2293-2019·2019-08-28
DeRoyal Enteral Safe Feeding Tubes Recalled for Connector Detachment
DeRoyal Industries is recalling specific polyurethane feeding tubes because the connector may detach from the tube.
Product
DeRoyal Enteral Safe Feeding Tubes: a) REF 54-2450R, 5 FR x 24" Polyurethane b) REF 54-2465R, 6.5 FR x 24" Polyurethane c) REF 54-2480R, 8 FR x 24" Polyurethane d) REF 54-3680R, 8 FR x 36" Polyurethane Product Usage: Feeding tube
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2065-2019·2019-08-28
Green Water LLC Recalls Multiple Herbal Tinctures and Teas Due to Salmonella Risk
Green Water, LLC is recalling specific lots of herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Product
Taspens Organics, Organic Tea: Respiratory, 2 ounce.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2292-2019·2019-08-28
Luminex Aries M1 Barcode Scanner Recall for Sample Mismatch Risk
Luminex is recalling Aries M1 barcode scanners due to incorrect control boards that could cause patient sample mismatches or duplicate results.
Product
Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in clinical laboratories. Scanner Label/Labeling: JADAK JDK-2330 REV B 170512-017
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2298-2019·2019-08-28
BD Vacutainer Lithium Heparin Tubes Recalled for False COHb Results
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Product
BD Vacutainer Lithium HeparinN (LH) 158 USP Units Blood Collection Tubes, Catalog Number 367880
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2309-2019·2019-08-28
BD Vacutainer Tubes Recalled for False Carboxyhemoglobin Results
Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they can cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer LH (Lithium Heparin) 68 I.U. Plus Blood Collection Tubes, Catalog Number 368884
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2305-2019·2019-08-28
BD Vacutainer Blood Collection Tubes Recalled for False COHb Results
Becton Dickinson is recalling specific blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 Units Blood Collection Tubes, Catalog Number 367964
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2304-2019·2019-08-28
BD Vacutainer Blood Collection Tubes Recalled for False COHb Results
Becton Dickinson is recalling specific blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Gel and Lithium HeparinN (LH) Blood Collection Tubes, Catalog Number 367963
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2303-2019·2019-08-28
BD Vacutainer Tubes Recalled for False Carboxyhemoglobin Results
Becton Dickinson is recalling specific blood collection tubes because they may cause falsely elevated carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection Tubes, Catalog Number 367962
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2353-2019·2019-08-28
Siemens ACUSON NX3 Ultrasound Systems Recalled for Acoustic Output Power Defect
Siemens is recalling ACUSON NX3 Elite ultrasound systems because internal testing found transducers may exceed defined acoustic output power values.
Product
ACUSON NX3 Elite Diagnostic Ultrasound System, Model # 11235411, RX Only, Siemens Medical Solutions, containing software versions: VA10A, VA10B, VA10C, VA10D, VA10E, VA10F, VB20A, and VB20B; UDI # 04056869004303 The ACUSON NX2 diagnostic ultrasound imaging systems are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2057-2019·2019-08-28
Keto Farms Strawberry Gouda Snack Mix Recalled for Undeclared Coconut
Keto Farms is recalling Strawberry Gouda snack mix because an inspection found undeclared coconut on the label.
Product
Keto Farms Keto Snack Mix - Strawberry Gouda; Fruit & Cheese Mix with Sprouted Pecans & Almonds; Net Wt. 95 g (3.34 oz.) Ingredients: Gouda Cheese (Pasteurized Milk, Cheese Culture, Salt, Enzymes), Sprouted Organic Pecans, Sprouted Transitional Almonds, Strawberries, MCT…
Category
Food
Distribution
Distributed nationwide
HighNHTSA·19V627000·2019-08-28
Toyota and Pontiac Recall Vehicles for Front Passenger Air Bag Defect
Toyota and GM are recalling specific Corolla, Corolla Matrix, and Pontiac Vibe vehicles because the front passenger air bag may not inflate properly in high temperatures.
Product
PONTIAC — PONTIAC, TOYOTA VIBE, COROLLA, COROLLA MATRIX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-2062-2019·2019-08-28
Green Water Recalls Multiple Herbal Tinctures and Teas for Salmonella Risk
Green Water, LLC is recalling several herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Product
Taspen s Organics,Digest Ease Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2063-2019·2019-08-28
Green Water Recalls Multiple Herbal Tinctures and Teas Due to Salmonella Risk
Green Water, LLC is recalling several herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Product
Taspen s Organics,Happy Momma Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2059-2019·2019-08-28
Keto Farms Recalls Raspberry Gouda Snack Mix for Undeclared Coconut
Keto Farms LLC is recalling its Raspberry Gouda Fruit & Cheese Mix because an inspection found that coconut, a declared allergen, was missing from the label.
Product
Keto Farms Keto Snack Mix - Raspberry Gouda Fruit & Cheese Mix with Sprouted Almonds & Walnuts; Net Wt. 95 g (3.34 oz. Ingredients: Gouda Cheese (Pasteurized Milk, Cheese Culture, Salt, Enzymes), Sprouted Organic Walnuts, Sprouted Transitional Almonds, Raspberries…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-2078-2019·2019-08-28
Hannaford Quiche Recalled for Missing Allergen Labeling
Meninno Brothers Gourmet Foods is recalling Hannaford brand quiche because the label lacks an ingredient or allergen statement.
Product
Hannaford brand 20 oz. traditional quiche w/tomatoes, cheese and basil in flexible plastic with round top and bottom.
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-2302-2019·2019-08-28
BD Vacutainer Blood Collection Tubes Recalled for False COHb Results
Becton Dickinson is recalling specific blood collection tubes because they can cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Product
BD Vacutainer PST Gel and Lithium HeparinN (LH) 65 Units Blood Collection Tubes, Catalog Number 367961
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2350-2019·2019-08-28
Siemens ACUSON NX2 Ultrasound Systems Recalled for Acoustic Output Power Defect
Siemens is recalling ACUSON NX2 ultrasound systems because internal testing found transducers may exceed defined acoustic output power values.
Product
ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software version VA10A, VA10B, VA11A, VA11B; UDI # 04056869030005 The ACUSON NX2 diagnostic ultrasound imaging systems are intended for the following applications…
Category
Medical Device
Distribution
Distributed nationwide