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.

2626–2650 of 80755

HighFDA (Devices)·Z-1654-2026·2026-04-08
Paradise renal denervation catheter unit distributed despite scrapping designation
One Paradise Ultrasound Renal Denervation catheter was distributed although it was a nonconforming product that should have been scrapped and not used in humans.
Product
Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0408-2026·2026-04-08
Amneal tramadol tablets failed nitrosamine impurity specification at stability
Amneal Pharmaceuticals is recalling two lots of Tramadol Hydrochloride Tablets 50 mg after a nitrosamine impurity was found out of specification at the 24-month stability interval.
Product
TRAMADOL HYDROCHLORIDE — TRAMADOL HYDROCHLORIDE (TRAMADOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1694-2026·2026-04-08
Olympus SOLTIVE Premium laser power supply may fail producing smoke
Olympus is recalling SOLTIVE Premium SuperPulsed Laser Systems because a potential defect in the 24V power supply module may render the system inoperable and produce smoke or a burning smell.
Product
Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/Catalog Number: TFL-PLS containing TFL-CPLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1680-2026·2026-04-08
Philips Azurion 5 M20 X-ray may not start from foot switch
Philips is recalling the Azurion 5 M20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1768-2026·2026-04-08
Monoject tuberculin syringe packages actually contain U-100 insulin syringes
Cardinal Health is recalling two lots of Monoject Tuberculin Syringes because the packaging identifies them as 1 mL Luer Lock tuberculin syringes but the contents are U-100 insulin syringes.
Product
Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777
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-1706-2026·2026-04-08
Medline bronchoscopy packs contain recalled Olympus biopsy valves shedding fragments
Medline is recalling three bronchoscopy convenience kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK, DYKE2096 2. NON MB BRONCHOPSCOPY CCH LH PK, DYNJT6182 3. PULMONARY BRONCH PACK, DYNDA2861A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1695-2026·2026-04-08
Olympus SOLTIVE Pro laser power supply may fail producing smoke
Olympus is recalling SOLTIVE Pro SuperPulsed Laser Systems because a potential defect in the 24V power supply module may render the system inoperable and produce smoke or a burning smell.
Product
Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TFL-CSLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1708-2026·2026-04-08
Medline endoscopy kits contain recalled Olympus biopsy valves shedding fragments
Medline is recalling BAL and ENDO 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. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
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 (Devices)·Z-1660-2026·2026-04-08
Philips Allura Xper FD10F X-ray may not start from foot switch
Philips is recalling the Allura Xper FD10F because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD10F; System Code: 722002;
Category
Medical Device
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-1670-2026·2026-04-08
Philips Allura Xper FD20/20 OR Table X-ray may not start
Philips is recalling the Allura Xper FD20/20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Allura Xper FD20/20 OR Table; System Code: 722039;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1690-2026·2026-04-08
Medline ENFit G-tube connectors may leak from dimensional specification failure
Medline is recalling ENFit G-tube connectors because they were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices.
Product
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1677-2026·2026-04-08
Philips Azurion 7 M12 X-ray may not start from foot switch
Philips is recalling the Azurion 7 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1747-2026·2026-04-08
MiniMed 620G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 620G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 620G Insulin Pump (MMT-1750)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1679-2026·2026-04-08
Philips Azurion 5 M12 X-ray may not start from foot switch
Philips is recalling the Azurion 5 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 5 M12; System Code: (1)722227, (2)722231;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1739-2026·2026-04-08
MiniMed 670G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 670G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1675-2026·2026-04-08
Philips Azurion 7 B12 X-ray may not start from foot switch
Philips is recalling the Azurion 7 B12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1691-2026·2026-04-08
Medline ENFit G-tube connector kits may leak from dimensional defect
Medline is recalling kits containing ENFit G-tube connectors because the connectors were not made to required dimensional specifications and may not form a proper seal.
Product
Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCHARGE KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1764-2026·2026-04-08
Burlington Medical blockers may lose radiation attenuation over time
Burlington Medical is recalling blockers because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Blockers.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1664-2026·2026-04-08
Philips Allura Xper FD20 Biplane X-ray may not start reliably
Philips is recalling the Allura Xper FD20 Biplane because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.
Product
ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1749-2026·2026-04-08
Paradigm REAL-Time insulin pump delivery varies with pump height
Medtronic is recalling Paradigm REAL-Time insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1762-2026·2026-04-08
Burlington Medical half aprons may lose radiation attenuation over time
Burlington Medical is recalling half aprons because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Half Aprons.
Category
Medical Device
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