California recalls
4272 federal recalls on file affecting California - 1197 California-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical devices
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat 5mm instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat devices
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceOlympusClass IINationwideStop using Olympus Thunderbeat surgical instruments
Firm is initiating a removal due to continued reports of adverse events.
- 2026-02-25FDA-DeviceMedicaClass IINationwideStop using Medica capillary tubes
A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica s capillary tubes.
- 2026-02-25FDA-DeviceImmunotechClass IINationwideStop using Immunotech Estrone RIA kits
The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very rare) cases may the issue occur.
- 2026-02-25FDA-DeviceBardClass IINationwideStop using affected Bard Broviac and Hickman catheters
Due to damage to outer tray that can potentially compromise the sterile barrier
- 2026-02-25FDA-DeviceMedlineClass IINationwideStop using Medline IV administration sets
Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets may leak, crack, and/or break during use, which may result in a delay in patient treatment, blood loss, infection, an air embolism, and/or underdosage of medication.
- 2026-02-25FDA-DeviceIntegra LifeSciencesClass IINationwideStop using CVS wound care gel model CVS405406
Potential packaging failures, which could lead to a breach in the sterile barrier.
- 2026-02-25FDA-DeviceIntegra LifeSciencesClass IINationwideStop using affected MEDIHONEY calcium alginate dressings
Potential packaging failures, which could lead to a breach in the sterile barrier.
- 2026-02-25FDA-DeviceIntegra LifeSciencesClass IINationwideStop using Integra MediHoney Gel dressing
Potential packaging failures, which could lead to a breach in the sterile barrier.
- 2026-02-25FDA-DeviceWilson-CookClass IIStop using Wilson-Cook Teslatome Sphincterotomes
Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting.
- 2026-02-25FDA-DeviceOlympusClass INationwideContact Olympus about UHI-3 insufflation unit recall
Issue with software algorithm which may lead to overpressure events.
- 2026-02-25FDA-DeviceOlympusClass INationwideStop using Olympus UHI-2 insufflation units
Issue with software algorithm which may lead to overpressure events.
- 2026-02-25FDA-DeviceOlympusClass INationwideStop using Olympus insufflation unit Model UHI
Issue with software algorithm which may lead to overpressure events.
- 2026-02-25FDA-FoodReser's Fine Foods, Inc.Class IStop using Molly Kitchen's Tuna Salad
Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad.
- 2026-02-25FDA-FoodIndian Kitchen MartClass IStop using Indian Kitchen Mart brass pot
Potential contamination with leachable lead.
- 2026-02-25FDA-FoodIndian Kitchen MartClass IIStop using Indian Kitchen Mart A-Cook kadai
Potential contamination with leachable lead.
- 2026-02-25FDA-FoodIndian Kitchen MartClass IIStop using Lotus Mom brass tope
Potential contamination with leachable lead.
- 2026-02-25FDA-FoodIndian Kitchen MartClass IIStop using Indian Kitchen Mart 9" saucepan
Potential contamination with leachable lead.
- 2026-02-25FDA-FoodWhy Not NaturalClass INationwideStop using Why Not Natural Moringa Capsules
Potential to be contaminated with Salmonella
- 2026-02-24CPSCYiruikeji2024NationwideStop using Yiruikeji2024 magnetic chess games
The recalled magnetic chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
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