Louisiana recalls
3482 federal recalls on file affecting Louisiana - 407 Louisiana-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath A2666T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath Model A2642
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath Model A2641
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Model A37004A sheaths
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideContact Olympus about recalled urological sheath
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus resection sheath Model A2666
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus WA22017T inner sheath
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath WA22017A
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath Model A4741
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath Model A42011A
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Inner Sheath Model A2660
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath A22043T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath 28 Fr.
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath A22042T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath Model A22042A
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath Model A22041T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath 24 Fr
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Inner Sheath A22040T
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Inner Sheath Model A22040A
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Resection Sheath immediately
Complaints of the ceramic tip of the resection sheath breaking have been received.
- 2026-03-04FDA-DeviceOlympusClass IINationwideStop using Olympus Cystoscope Outer Sheath WA22810A
Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
- 2026-03-04FDA-DeviceMRIMedClass IINationwideStop using MRIMed SL-111 exam light batteries
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Meijer saline wound wash spray
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Medline Nail Kit DYKM1528
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Medline Convenience Kits
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Medline Convenience Nail Kit
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Medline Sterile Saline Wound Wash
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
- 2026-03-04FDA-FoodTENGEN USA TRADING CORPClass IIIStop eating YO!MAN Lettuce Spicy Flavor
Product contains undeclared cyclamates.
- 2026-03-04FDA-FoodTengen USA TradingClass IIIDo not eat YO!MAN Cucumber products
Product contains undeclared cyclamates.
- 2026-03-04FDA-FoodLubna Quality ProductsClass IIIStop using Lubna Quality Products mung beans
Presence of Thiamethoxam-PESTICIDE
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