State

Tennessee product recalls

72,936 recalls have nationwide distribution and so reach Tennessee. 7,819 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,819
Critical: 1,317
Severe: 1,653
Most recent: 2026-09-09

Of the 7,819 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 7,819 recalls whose distribution notice names Tennessee specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2576–2600 of 80755

HighFDA (Devices)·Z-1710-2026·2026-04-08
Medline bronchoscopy kits contain Olympus biopsy valves that shed fragments
Medline is recalling six bronchoscopy and thoracic kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT, DYKE2091 2. BRONCHSCOPY, DYNJ900898G DYNJ901922I 3. BRONCHSCOPY PACK, DYNJ38313B 4. BRONCHOSCOPY PACK 0120367-LF, DYNJ32750G DYNJ32750I 5. KIT, WR THORACIC, DYNJ911252 6. LARYNGOSCOPY/BRON
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1753-2026·2026-04-08
Burlington Medical thyroid shields may lose radiation attenuation over time
Burlington Medical is recalling thyroid shields over the potential for attenuation degradation over time, which decreases the product's usable lifespan. 41,962 units are affected.
Product
Burlington Medical, Thyroid Shield.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1665-2026·2026-04-08
Philips Allura Xper FD20 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1744-2026·2026-04-08
MiniMed 700G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 700G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0638-2026·2026-04-08
Dumpling and Loaded Dumpling Vegetable products recalled for glass contamination
JFE Franchising Inc is recalling Dumpling Vegetable and Loaded Dumpling Vegetable products due to the presence of glass fragments. The products were distributed across multiple U.S. states.
Product
" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1703-2026·2026-04-08
VOLT bone taps swapped between lots carry the incorrect thread
The 2.4 VOLT Tap Cortex Screw is being recalled after a full lot swap with the VOLT Locking Screw Tap left the bone taps with an incorrect thread.
Product
2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1700-2026·2026-04-08
da Vinci tenaculum forceps recalled over frayed or broken pitch cables
Intuitive Surgical is recalling da Vinci S and Si Tenaculum Forceps Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp end
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1698-2026·2026-04-08
da Vinci mega needle driver recalled over broken or frayed cables
Intuitive Surgical is recalling da Vinci S and Si Mega Needle Driver Instruments following increased complaints of broken or frayed grip cables in reusable instruments.
Product
Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1761-2026·2026-04-08
Burlington Medical leg wraps may lose radiation attenuation over time
Burlington Medical is recalling leg wraps because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Leg Wraps.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0419-2026·2026-04-08
Prazosin hydrochloride 100-count bottles recalled over nitrosamine impurity
A further quantity of Prazosin Hydrochloride tablets is being recalled after detection of the nitrosamine impurity N-nitroso-prazosin impurity C above acceptable limits.
Product
PRAZOSIN HYDROCHLORIDE — PRAZOSIN HYDROCHLORIDE (PRAZOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0420-2026·2026-04-08
Prazosin hydrochloride tablets recalled over nitrosamine impurity above limits
Five lots of Prazosin Hydrochloride tablets are being recalled after detection of the nitrosamine impurity N-nitroso-prazosin impurity C above acceptable limits.
Product
PRAZOSIN HYDROCHLORIDE — PRAZOSIN HYDROCHLORIDE (PRAZOSIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1711-2026·2026-04-08
Medline anterior hip pack contains recalled Olympus biopsy valves
Medline is recalling the Anterior Hip Pack because it contains recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
MEDLINE ANTERIOR HIP PACK DYNJ64672B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1701-2026·2026-04-08
da Vinci permanent cautery hook recalled over frayed pitch cables
Intuitive Surgical is recalling da Vinci S and Si Permanent Cautery Hook Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Product Description: EndoWrist Instruments or da Vinci S/Si Reusable instruments, including blunt and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1684-2026·2026-04-08
CPX 4 tall height tissue expander infusion needles may be blunt
Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the smooth tall height range because the infusion sets may contain a dull or blunt needle tip.
Product
CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-113TH, SCPX-123TH, SCPX-140TH, SCPX-146TH Smooth Tall Height Tissue Expander, 350cc, 450cc, 650cc, 750cc
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1755-2026·2026-04-08
Burlington Medical kilts may lose radiation attenuation over time
Burlington Medical is recalling kilts made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
Product
Burlington Medical, Kilt
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1681-2026·2026-04-08
CPX 4 SILTEX low height expander infusion needles may be blunt
Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the SILTEX low height range because the infusion sets may contain a dull or blunt needle tip.
Product
CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113, 3549313, 354-9314 SILTEX Low Height Tissue Expander Style (9100, 450cc), (9300, 450cc), (9300, 550cc)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1746-2026·2026-04-08
MiniMed 740G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 740G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1751-2026·2026-04-08
MiniMed 530G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 530G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 530G Insulin Pump (MMT-551, MMT-751)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1707-2026·2026-04-08
Medline thoracic robot kits contain recalled Olympus biopsy valves
Medline is recalling Thoracic Robots kits, model DYNJ908777B, because they contain recalled Olympus biopsy valves where rubber fragments may detach from the valve slit.
Product
THORACIC ROBOTS, DYNJ908777B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1754-2026·2026-04-08
Burlington Medical radiation protection vests may lose attenuation over time
Burlington Medical is recalling protective vests because of the potential for attenuation degradation over time, decreasing the lifespan of the garment.
Product
Burlington Medical, Vest
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0660-2026·2026-04-08
Imu-Tek Colostrum-5 Capsules Recalled for Potential Under-Processing
Imu-Tek Animal Health is recalling Imu-Tek Colostrum-5 120 Capsules (Lot #013, Expiration 092826) because the product is potentially under-processed. The product was distributed across 29 states.
Product
Imu-Tek Colostrum-5 120 Capsules; 30% IgG, 2 capsules 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band seal, 500 mg capsule, 7 38654 00026 7, Imu-Tek, Inc. Ft. Collins, CO 80524.
Category
Food
Distribution
30 states
HighFDA (Devices)·Z-1692-2026·2026-04-08
Vue Motion V12 may display cine image frames out of sequence
Philips is recalling Vue Motion V12 because mis-ordered frames during dynamic cine runs may cause image frames to display out of sequence.
Product
Vue Motion V12. Product Number: 1017979.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1693-2026·2026-04-08
Sterile radiology procedure kits may have a breached sterile pouch
One lot of Sterile Radiology Procedure Kits, model DYNDH1491B, is being recalled because of a potential breach in the sterile pouch packaging that may compromise sterility.
Product
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0637-2026·2026-04-08
Divided Sunset Multi Collagen Peptides Missing Allergen Labeling
TG FOODS INC is recalling Divided Sunset Multi Collagen Peptides (8 oz) because the product contains eggshell membrane collagen and wild-caught marine collagen but fails to declare EGG and the specific fish species on the label.
Product
Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Pouch, UPC Code: 8 50005 60689 5
Category
Food
Distribution
28 states
HighFDA (Devices)·Z-1767-2026·2026-04-08
GE SIGNA Premier MRI magnets may have ferrous fittings fitted
SIGNA Premier MRI systems are being recalled because they may have been built or serviced with ferrous steel fittings instead of non-ferrous brass on the magnet rear.
Product
SIGNA Premier systems
Category
Medical Device
Distribution
Distributed nationwide