The Recall Desk

State

California product recalls

72,933 recalls have nationwide distribution and so reach California. 13,245 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total
13,245
Critical
1,605
Severe
2,843
Most recent
2026-09-09

Of the 13,245 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,843 (21%) are Severe.

Which agencies issued them

These figures cover only the 13,245 recalls whose distribution notice names California specifically. The 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2726–2750 of 86178

  • HighFDA (Devices)·Z-1696-2026·2026-04-08

    da Vinci monopolar curved scissors recalled over frayed grip cables

    Intuitive Surgical is recalling da Vinci S and Si Monopolar Curved Scissors Instruments following increased complaints of broken or frayed grip cables in reusable instruments.

    Product
    Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved Scissors Instrument Model/Catalog Number: 420179 Software Version: N/A Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including
    Category
    Medical Device
    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 (Food)·H-0646-2026·2026-04-08

    Coconut Drink 1 recalled due to undeclared milk allergen

    HEYTEA USA INC is recalling Coconut Drink 1 (1L cartons) because the product contains undeclared milk. Consumers with milk allergies or sensitivities are at risk.

    Product
    Coconut Drink 1; NET VOLUME: 1L; Ingredients: Coconut water, freshly squeezed coconut gravy, white granulated sugar, emulsion stabilizer [sodium caseinate, mono- and diglycerides fatty acid esters, sucrose fatty acid esters]; Storage Condition: Room temperature; Manufactured in:
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·H-0637-2026·2026-04-08

    Divided Sunset Multi Collagen Peptides Missing Allergen Labeling

    TG FOODS INC is recalling Divided Sunset Multi Collagen Peptides (8 oz) because the product contains eggshell membrane collagen and wild-caught marine collagen but fails to declare EGG and the specific fish species on the label.

    Product
    Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Pouch, UPC Code: 8 50005 60689 5
    Category
    Food
    Distribution
    28 states
  • HighFDA (Devices)·Z-1698-2026·2026-04-08

    da Vinci mega needle driver recalled over broken or frayed cables

    Intuitive Surgical is recalling da Vinci S and Si Mega Needle Driver Instruments following increased complaints of broken or frayed grip cables in reusable instruments.

    Product
    Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1741-2026·2026-04-08

    MiniMed 780G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 780G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1681-2026·2026-04-08

    CPX 4 SILTEX low height expander infusion needles may be blunt

    Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the SILTEX low height range because the infusion sets may contain a dull or blunt needle tip.

    Product
    CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113, 3549313, 354-9314 SILTEX Low Height Tissue Expander Style (9100, 450cc), (9300, 450cc), (9300, 550cc)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1750-2026·2026-04-08

    Paradigm REAL-Time Revel pump delivery varies with pump height changes

    Medtronic is recalling Paradigm REAL-Time Revel 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 Revel Insulin Pump (MMT-523, MMT-723)
    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
  • 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-1757-2026·2026-04-08

    Burlington Medical wrap aprons may lose radiation attenuation over time

    Burlington Medical is recalling wrap aprons made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.

    Product
    Burlington Medical, Wrap Aprons.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1761-2026·2026-04-08

    Burlington Medical leg wraps may lose radiation attenuation over time

    Burlington Medical is recalling leg wraps because of the potential for attenuation degradation over time, decreasing the lifespan of the product.

    Product
    Burlington Medical, Leg Wraps.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1685-2026·2026-04-08

    Artoura textured tissue expander infusion set needles may be blunt

    Mentor is recalling textured Artoura Breast Tissue Expanders with integral injection dome because the infusion sets may contain a dull or blunt needle tip.

    Product
    Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra High Profile, Integral Injection Dome, 300cc, 375cc, 535cc, 475cc, 500cc, 600cc, 750cc,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0638-2026·2026-04-08

    Dumpling and Loaded Dumpling Vegetable products recalled for glass contamination

    JFE Franchising Inc is recalling Dumpling Vegetable and Loaded Dumpling Vegetable products due to the presence of glass fragments. The products were distributed across multiple U.S. states.

    Product
    " Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953
    Category
    Food
    Distribution
    37 states
  • 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-1745-2026·2026-04-08

    MiniMed 720G insulin pump delivery varies with pump height changes

    Medtronic is recalling MiniMed 720G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.

    Product
    MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1756-2026·2026-04-08

    Burlington Medical frontal aprons may lose radiation attenuation over time

    Burlington Medical is recalling frontal aprons made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.

    Product
    Burlington Medical, Frontal Aprons
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1678-2026·2026-04-08

    Philips Azurion 7 M20 X-ray may not start from foot switch

    Philips has identified instances where X-ray imaging on the Azurion 7 M20 may not initiate, or may run intermittently, when the wired foot switch is used. 5,167 units are affected.

    Product
    Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1755-2026·2026-04-08

    Burlington Medical kilts may lose radiation attenuation over time

    Burlington Medical is recalling kilts made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.

    Product
    Burlington Medical, Kilt
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1683-2026·2026-04-08

    CPX 4 medium height tissue expander infusion needles may be blunt

    Mentor is recalling CPX 4 US Breast Tissue Expanders with Suture Tabs in the smooth medium height range because the infusion sets may contain a dull or blunt needle tip.

    Product
    CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth Medium Height Tissue Expander, 275cc, 350cc, 450cc, 550cc, 650cc, 800cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V221000·2026-04-08

    Forest River Recalls 2026 Travel Trailers Due to Incorrect Weight Labeling

    Forest River is recalling 2026 Westbrook and Avenger travel trailers because the Federal Placard label may list an incorrect dry weight, potentially leading to vehicle overloading.

    Product
    FOREST RIVER — FOREST RIVER AVENGER, WESTBROOK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0636-2026·2026-04-08

    Popping Boba Ready-to-Drink Mango Passion Fruit Green Tea Recall

    Pocas International Corp. is recalling Popping Boba RTD Mango Passion Fruit Green Tea due to a packaging integrity issue that may compromise product quality.

    Product
    POPPING BOBA RTD MANGO PASSION FRUIT GREEN TEA 12 X 13.8OZ
    Category
    Food
    Distribution
    8 states