State

Tennessee product recalls

72,971 recalls have nationwide distribution and so reach Tennessee. 7,821 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,821
Critical: 1,317
Severe: 1,653
Most recent: 2026-09-16

Of the 7,821 recalls naming Tennessee we have scored against our rubric, 1,317 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,653 (21%) are Severe.

Which agencies issued them

These figures cover only the 7,821 recalls whose distribution notice names Tennessee specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5701–5725 of 80792

ModerateFDA (Devices)·Z-2477-2025·2025-09-03
Medication dispensing stations recalled because antivirus software was not consistently installed
BD Pyxis MedStation and Anesthesia Station devices are recalled because antivirus software was not consistently installed during implementation. 8,353 devices are affected, 6,738 of them in the US.
Product
BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis" MedStation" ES Tower / 10885403512674 / 352 BD Pyxis" Anesthesia Station ES / 10885403477836 / 327 BD Pyxis" MedStation" ES (Main) / 10885403512667 / 323
Category
Medical Device
Distribution
Distributed nationwide
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-2475-2025·2025-09-03
Anti-Xa test kits recalled over potential contamination by fibrinogen reagents
STA-Liquid Anti-Xa 8 kits are recalled because of the potential for contamination by Stago Fibrinogen reagents in unfractionated and low molecular weight heparin applications. 126,200 units are affected.
Product
STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid Anti-Xa kits are intended for use with STA-R, STA Compact and STA Satellite analyzers, for the quantitative determination of the plasma levels of unfractionated (UFH) and low molecular weight (LMWH) heparin
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2396-2025·2025-09-03
S7-2t ultrasound probes recalled for useful life labelling in the field
S7-2t 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
S7-2t Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2353-2025·2025-09-03
C5-2 transducer probes recalled over ultrasound useful life labelling clarification
C5-2 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
C5-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2386-2025·2025-09-03
mL26-8 transducer probes recalled to add field useful life labelling
mL26-8 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
mL26-8 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2364-2025·2025-09-03
C9-4v transducer probes recalled for useful life labelling clarification
C9-4v 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
C9-4v Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2374-2025·2025-09-03
L12-4 Lumify transducer probes recalled to clarify device useful life
L12-4 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
L12-4 Lumify Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2385-2025·2025-09-03
Mini Multi TEE transducer probes recalled to clarify useful life labelling
Mini Multi 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
Mini Multi TEE Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2412-2025·2025-09-03
X7-2t transducer probes recalled to add useful life labelling information
X7-2t 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
X7-2t 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-2403-2025·2025-09-03
V6-2 transducer probes recalled to clarify useful life in the field
V6-2 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
V6-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2376-2025·2025-09-03
L12-5 50 transducer probes recalled to define ultrasound transducer useful life
L12-5 50 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
L12-5 50 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2346-2025·2025-09-03
3D6-2 transducer probes recalled to add field useful life labelling
3D6-2 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
3D6-2 Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2463-2025·2025-09-03
Leg massagers recalled over documentation error and misleading color packaging claim
HoMedics Air Compression Leg Massagers, model SR-160HJ, are recalled for a regulatory documentation error and a misleading color packaging claim. The record states the affected lots do not present a risk of harm.
Product
Brand Name: HOMEDICS Product Name: Air Compression Leg Massager Model/Catalog Number: SR-160HJ Product Description: Powered Inflatable Tube Massager used on the leg. The Air Compression Leg Massager is indicated for the temporary relief of minor muscle aches and pains and f
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
LowFDA (Devices)·Z-2383-2025·2025-09-03
mC12-3 ultrasound probes recalled for labelling defining device useful life
mC12-3 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
mC12-3 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-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-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-2375-2025·2025-09-03
L12-5 38mm transducer probes recalled to add useful life labelling
L12-5 38mm 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
L12-5 38mm Transducer Probe
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2347-2025·2025-09-03
3D9-3v ultrasound transducer probes recalled for useful life labelling clarification
3D9-3v 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
3D9-3v 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-2408-2025·2025-09-03
X5-1 transducer probes recalled to clarify useful life in the field
X5-1 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
X5-1 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