The Recall Desk

State

California product recalls

73,088 recalls have nationwide distribution and so reach California. 13,251 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total
13,251
Critical
1,605
Severe
2,846
Most recent
2026-09-25

Of the 13,251 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 2,846 (21%) are Severe.

These figures cover only the 13,251 recalls whose distribution notice names California specifically. The 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9726–9750 of 86339

  • HighFDA (Devices)·Z-0537-2025·2024-12-04

    Philips dS Breast 16ch 1.5T MRI Recalled for Patient Safety Risk

    Philips North America is recalling approximately 5,231 dS Breast 16ch 1.5T MRI systems nationwide due to a potential safety issue that could harm patients during scan preparation or procedures.

    Product
    dS Breast 16ch 1.5T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0511-2025·2024-12-04

    MEDLINE ultrasound procedure kit connectors recalled due to insertion malfunction

    Medline Industries is recalling procedure kits with connectors that may fail to open fully, preventing proper catheter insertion. The recall affects 3,396 units distributed in the U.S. and internationally.

    Product
    MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0513-2025·2024-12-04

    MEDLINE Epidural and Spinal Procedure Kits: Connector May Prevent Catheter Insertion

    MEDLINE is recalling 3,744 epidural and spinal procedure kits due to a connector defect that may prevent proper catheter insertion. Affected kits were distributed nationwide and internationally.

    Product
    MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; 2) CSE TRAY, REF PAIN1941; 3) TRAY CON EPID 20G NYL W/TUOHY, REF PAIN9023; 4) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN1281 5) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN9024
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0158-2025·2024-12-04

    KRUSTEAZ Griddle Pancake Mix Recalled Nationwide for Potential Listeria Contamination

    Treehouse Foods is recalling KRUSTEAZ Griddle Pancake Mix due to potential Listeria monocytogenes contamination. Approximately 9,907,389 cases with batch codes starting with '2C' and Best By dates from October 1, 2024, through October 11, 2025, are affected.

    Product
    KRUSTEAZ 12/15oz GRDL PNCK MINI BTRMLK-KTZCM UPC 686151200164
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0167-2025·2024-12-04

    Gordon Food Service Waffle Mix Recalled Due to Potential Listeria Contamination

    Treehouse Foods is recalling 9.9 million cases of Gordon Food Service waffle mix due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 2024 to October 2025.

    Product
    GORDON FOOD SERVICE 1/10.8lb GRDL WFL BLGN BFFT - GDNFS
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0166-2025·2024-12-04

    Nature's Path Organic Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Nature's Path Organic Griddle Waffles (9,907,389 cases) for potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates from October 1, 2024 through October 11, 2025.

    Product
    NATURES PATH ORGANIC 12/7.4oz GRDL WFL BCKWHE BRY ORG GF-NPTHO UPC 058449590583 NATURES PATH ORGANIC 12/210g GRDL WFL BCKWHE BRY ORG GF-NPOCN UPC 058449590576
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0542-2025·2024-12-04

    Mammotrak Interventional Coil 1.5T recalled for patient safety risk

    Philips is recalling 5,231 units of the Mammotrak Interventional Coil 1.5T nationwide due to a potential safety issue that may harm patients during MRI preparation or scanning.

    Product
    Mammotrak Interventional Coil 1.5T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0172-2025·2024-12-04

    Krusteaz Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Krusteaz 12-pack griddle waffles nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.

    Product
    KRUSTEAZ 12/9oz GRDL WFL BLBRY MINI-KRSTZ UPC 041820819120
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0151-2025·2024-12-04

    Treehouse Foods Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling BREAKFAST BEST griddle waffles nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates from October 1, 2024 through October 11, 2025.

    Product
    BREAKFAST BEST 12/13.4oz MXCS GRDL WFL PRTN 6BB 6BM-BKBST
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0169-2025·2024-12-04

    Kodiak Cakes Griddle Waffles Recalled Due to Listeria Risk

    Treehouse Foods recalls Kodiak Cakes 8/14.8oz Griddle Waffles due to potential Listeria monocytogenes contamination. Affected products carry batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.

    Product
    KODIAK CAKES 8/14.8oz GRDL WFL BLGN BLBRY-KDKCS UPC 705599014826
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0193-2025·2024-12-04

    Griddle Waffles with Flax Recalled Due to Listeria Contamination Risk

    Multiple brands of organic griddle waffles with flax are being recalled due to potential Listeria monocytogenes contamination. Affected products include Wegmans, H-E-B, Nature's Path Organic, and Central Market brands.

    Product
    WEGMANS 12/7.4oz GRDL WFL FLAX ORG - WEGMN UPC 077890481424 H-E-B 12/8.25oz GRDL WFL FLAX ORG-HEBUT UPC 041220708338 WEGMANS 12/8.25OZ 6CT GRDL WFL FLAX ORG-WEGMN UPC 077890577059 NATURES PATH ORGANIC 12/7.4oz GRDL WFL FLAX ORG - NPTHO UPC 058449590569 NATURES PATH ORGANIC 12/210
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0206-2025·2024-12-04

    Organic Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling organic griddle waffles sold under multiple brand names due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide in the USA and Canada.

    Product
    GOOD & GATHER 12/9oz GRDL WFL MINI HSTYLE ORG-GDGTR UPC 085239343029 H-E-B 12/9oz GRDL WFL MINI HSTYLE ORG-HEBUT UPC 041220708413 365 ORGANIC 12/9oz GRDL WFL MINI HSTYLE ORG - 365OR UPC 099482436995 WEGMANS 12/9oz GRDL WFL MINI HSTYLE ORG - WEGMN UPC 077890481448
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0207-2025·2024-12-04

    Kodiak Cakes Mini Griddle Waffles Recalled for Listeria Contamination Risk

    Treehouse Foods recalls Kodiak Cakes 8/9.88oz Mini Griddle Waffles sold nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates from October 1, 2024 through October 11, 2025.

    Product
    KODIAK CAKES 8/9.88oz GRDL WFL ORIG MINI-KDKCS UPC 705599017148
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0538-2025·2024-12-04

    Philips dS Breast MRI System Recalled for Patient Safety Hazard

    Philips dS Breast 16ch 3.0T MRI systems are being recalled due to a potential safety issue that could harm patients during medical scans. The FDA-mandated Class II recall affects 5,231 units distributed nationwide.

    Product
    dS Breast 16ch 3.0T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0514-2025·2024-12-04

    MEDLINE Neuraxial Kit Connectors May Prevent Catheter Insertion

    MEDLINE has recalled 360 units of its Neuraxial Kit (Lot 23KLA330) because connectors may not fully open, potentially preventing catheters from being inserted as intended. Healthcare facilities should discontinue use and contact MEDLINE.

    Product
    MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0532-2025·2024-12-04

    Medline Surgical Kits Recalled for Incorrect Needle and Suture Specifications

    Medline Industries is recalling 408 surgical kits from Alabama, Georgia, Massachusetts, New Jersey, and Pennsylvania. Some suture packages within the kits contain incorrect needle types and sizes, and incorrect suture diameters and lengths.

    Product
    (1) Medline Open Heart CDS, REF CDS840132O, packaged 1 kit/case, non-sterile; and (2) Medline Dr. Davies CV, REF DYNJ903016G, packaged 1 kit/case, non-sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0196-2025·2024-12-04

    Simple Truth Griddle Waffles Recalled for Potential Listeria Contamination

    Treehouse Foods is recalling Simple Truth griddle waffles with batch codes starting with 2C due to potential Listeria monocytogenes contamination. Approximately 9.9 million cases were distributed nationwide in the USA and Canada.

    Product
    SIMPLE TRUTH 12/11.3oz GRDL WFL HSTYLE GF-SMPTR UPC 011110105493
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0179-2025·2024-12-04

    Frozen Griddle and Belgian Waffle Products Recalled for Listeria Contamination Risk

    Treehouse Foods is recalling multiple frozen griddle and Belgian waffle brands nationwide due to potential Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    DUNCAN HINES 1/3.12kg GRDL WFL BLGN ORIG 4IN - DUNHN UPC 091479060275 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151903331 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG-KRSMX UPC 00686151805307 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151904017 GORDON CHOICE 1/3.12kg G
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0553-2025·2024-12-04

    Shimadzu Autosampler Water Intrusion May Cause Electrical Short Circuit

    Shimadzu laboratory autosamplers are being recalled due to water intrusion from a dehumidifier that can cause electrical short circuits. Affected units are distributed worldwide, including across the United States.

    Product
    Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0530-2025·2024-12-04

    AMS Artificial Urinary Sphincter Control Pump: Mislabeled Packaging Recall

    Boston Scientific recalled 16 units of AMS Artificial Urinary Sphincter Control Pumps due to mislabeled packaging where devices labeled as Pressure Regulating Balloons actually contained Control Pumps.

    Product
    AMS Artificial Urinary Sphincter Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0540-2025·2024-12-04

    Philips dS Breast 7ch 3.0T MRI Coil Recalled for Patient Safety Hazard

    Philips is recalling 5,231 dS Breast 7ch 3.0T breast MRI coils distributed nationwide due to a potential safety issue that may harm patients during scan preparation or scanning. The FDA classified this as Class II.

    Product
    dS Breast 7ch 3.0T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0545-2025·2024-12-04

    Philips SENSE Breast Coil Recall for Potential Patient Safety Hazard

    Philips is recalling 5,231 SENSE Breast Coils due to a potential patient safety hazard during scan preparation and performance. The FDA has not disclosed specific details about the nature of the risk.

    Product
    SENSE Breast Coil
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0535-2025·2024-12-04

    VITROS Chemistry CRP Diagnostic Slides May Underreport Elevated Results

    Ortho-Clinical Diagnostics is recalling 7,717 units of VITROS CRP diagnostic slides that may produce falsely low results for high C-reactive protein samples, risking missed diagnosis of infection or inflammation.

    Product
    VITROS Chemistry Products CRP Slides- In vitro diagnostic quantitatively measures C-reactive protein (CRP) concentration in serum and plasma Model/Catalog Number: 1926740
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0548-2025·2024-12-04

    Philips ST SENSE Breast Imaging Coil Recalled for Patient Safety Risk

    Philips is recalling 5,231 units of the ST SENSE Breast Dx Coil nationwide due to a potential safety issue that may harm patients during breast imaging scans. No injuries have been reported.

    Product
    ST SENSE Breast Dx Coil
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0518-2025·2024-12-04

    GE SIGNA Architect MRI Systems Recalled for Elevated Acoustic Noise

    GE Medical Systems is recalling certain SIGNA Architect MRI systems because their gradient coils can produce elevated acoustic noise during scanning under specific conditions, potentially risking hearing damage.

    Product
    SIGNA Architect, Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide