Texas recalls
4031 federal recalls on file affecting Texas - 956 Texas-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 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-DeviceHitachiClass IICheck Hitachi Proton Beam Therapy positioning
Software anomaly in the patient positioning system may result in positional discrepancy.
- 2026-03-04FDA-DeviceHitachiClass IICheck Hitachi proton therapy system positioning
Software anomaly in the patient positioning system may result in positional discrepancy.
- 2026-03-04FDA-FoodNavitasClass INAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA). Product of Mexico/Argentina/Paraguay. Distributed by Navitas Organics Novato, CA USA 94949 UPC: 858847000284
Potential contamination with Salmonella.
- 2026-03-04FDA-FoodKoi Koi TradingClass IStop using Koi Koi Trading frozen fish balls
Undeclared allergen ingredient (Wheat and Sesame)
- 2026-03-04FDA-FoodKoi Koi TradingClass IStop using Koi Koi Trading frozen fish balls
Undeclared allergen ingredient (Wheat and Sesame)
- 2026-03-04FDA-FoodKoi Koi TradingClass IStop using Koi Koi Trading frozen fish balls
Undeclared allergen ingredient (Wheat and Sesame)
- 2026-03-04FDA-FoodSB FoodClass IIStop eating Yoyo Gummy Grape Plus
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
- 2026-03-04FDA-FoodSB FoodClass IIStop eating Yoyo Gummy Tropical Flavor
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
- 2026-03-04FDA-FoodSB FoodClass IIStop eating Yoyo Gummy Assorted Flavor
The products contain an unallowed color Carmoisine (E122) - Acid Red 14.
- 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.
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