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.

5676–5700 of 81180

ModerateFDA (Devices)·Z-2418-2025·2025-09-03
NovoTHOR Gen 3.0 unit recalled because gas strut may detach from canopy
A single NovoTHOR Gen 3.0 Reg PRX unit, model S2189, is recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift.
Product
Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2189 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissu
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2417-2025·2025-09-03
NovoTHOR XL devices recalled over failed welded nut detaching gas strut
NovoTHOR XL devices, model S2190, are recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift. 55 units are affected.
Product
Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissue temperature
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2476-2025·2025-09-03
Fibrinogen test kits recalled over potential cross-contamination in heparin assays
STA-Fibrinogen 5 kits are recalled because of the potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in heparin applications. 829,800 units are affected, 245,200 of them in the US.
Product
STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Fibrinogen 5 kit is intended for use with the analyzers of the STA-R, STA Compact and STA Satellite families for the quantitative determination of fibrinogen levels in human citrated plasma by the clotting method of
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2421-2025·2025-09-03
Dental implant locating kits recalled over thread defect limiting full engagement
Atlantis IO FLO-S Kits are recalled because a thread defect stops the device fully engaging an implant or analog, engaging about two rotations instead of five. 102 units are affected.
Product
Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04B / 68020033 Software Version: n/a Product Description: The Atlantis intraoral feature locating object for suprastructures (IO FLO-S) is intended to support the prosthetic procedure wit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2416-2025·2025-09-03
NovoTHOR light therapy devices recalled over welded nut that may shear
NovoTHOR devices, model S2188, are recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift. 80 units are affected.
Product
Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissue temperature fo
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2362-2025·2025-09-03
C9-3v transducer probes recalled over useful life labelling clarification
C9-3v Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C9-3v Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2349-2025·2025-09-03
BP10-5ec ultrasound probes recalled for labelling defining device useful life
BP10-5ec Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
BP10-5ec Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2413-2025·2025-09-03
X8-2t ultrasound probes recalled for labelling defining device useful life
X8-2t Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
X8-2t Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2388-2025·2025-09-03
OMNI III TEE transducer probes recalled to add useful life labelling
OMNI III TEE Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
OMNI III TEE Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2398-2025·2025-09-03
S8-3t ultrasound probes recalled for labelling defining device useful life
S8-3t Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
S8-3t Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2373-2025·2025-09-03
L12-4 transducer probes recalled to define ultrasound transducer useful life
L12-4 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
L12-4 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2405-2025·2025-09-03
VL13-5 ultrasound transducer probes recalled to clarify device useful life labelling
VL13-5 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
VL13-5 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2399-2025·2025-09-03
S9-2 transducer probes recalled to clarify useful life in the field
S9-2 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
S9-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2359-2025·2025-09-03
C8-5 ultrasound probes recalled for labelling defining transducer useful life
C8-5 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C8-5 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2357-2025·2025-09-03
C8-4v transducer probes recalled to define ultrasound transducer useful life
C8-4v Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C8-4v Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2402-2025·2025-09-03
L12-5 transducer probe serial B1D3VM recalled over useful life labelling
The L12-5 Transducer Probe is the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
TRANSDUCER L12-5 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2378-2025·2025-09-03
L15-7IO transducer probe serial B1K740 recalled over useful life labelling
The L15-7IO Transducer Probe is the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
L15-7IO TRANSDUCER Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2354-2025·2025-09-03
C5-2 Lumify transducer probes recalled to add useful life labelling
C5-2 Lumify Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C5-2 Lumify Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2400-2025·2025-09-03
L7-4 HDI transducer probes recalled to clarify device useful life
SCNHD LA L7-4 HDI Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
SCNHD LA L7-4 HDI Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2348-2025·2025-09-03
7.5 MHz Endo transducer probes recalled to clarify useful life labelling
The 7.5 MHz Endo Transducer Probe is the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
7.5MHZ Endo Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2351-2025·2025-09-03
C10-4ec ultrasound transducer probes recalled to add useful life labelling
C10-4ec Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C10-4ec Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2381-2025·2025-09-03
L8-4 transducer probes recalled to add field useful life labelling
L8-4 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
L8-4 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2380-2025·2025-09-03
L18-5 ultrasound transducer probes recalled to add useful life labelling
L18-5 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
L18-5 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2358-2025·2025-09-03
C8-4v ultrasound transducer probes recalled to add useful life labelling
C8-4v Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
C8-4v Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2389-2025·2025-09-03
S12-4 transducer probes recalled to clarify useful life in the field
S12-4 Transducer Probes are the subject of a recall issued to provide clarification and labelling defining the useful life of ultrasound transducers in the field.
Product
S12-4 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide