Louisiana recalls
3482 federal recalls on file affecting Louisiana - 407 Louisiana-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-VC433Q-0730
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-VC433Q-0720
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideCheck Olympus sphincterotome model KD-VC412Q-0215
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-VC411Q-0330
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideCheck Olympus sphincterotome devices for deformation
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-VC411Q-0730
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using affected Olympus sphincterotome devices
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-VC431Q-0730
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-V431M-0730
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-V431M-0720
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-V411M-0730
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-V411M-0725
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome model KD-V411M-0720
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome devices
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus sphincterotome KD-431Q-0720
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus Sphincterotome V model KD-VC431Q-0720
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceOlympusClass IINationwideStop using Olympus CleverCut sphincterotome devices
Devices which did not undergo thermoforming could deform and lose performance.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using Vivoo test strips
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using Vivoo Vaginal pH Test strips
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using Vivoo Protein Test strips
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using Vivoo pH Test strips
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using Exploro fertility test strips
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using Changchun Wancheng sperm test kit
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using Changchun Wancheng typhoid test strips
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using Changchun Wancheng Menopause Test Cassette
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using LH One Step Ovulation Test
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using these urine test strips
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceChangchun WanchengClass IINationwideStop using recalled UTI test strips
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.
- 2026-02-11FDA-DeviceVortex SurgicalClass IINationwideStop using Vortex Surgical scleral markers
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.
- 2026-02-11FDA-DeviceVortex SurgicalClass IINationwideStop using Vortex Surgical 25GA and 27GA Backflush needles
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.
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