The Recall Desk

State

California product recalls

72,940 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.

These figures cover only the 13,245 recalls whose distribution notice names California specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5126–5150 of 86185

  • ModerateFDA (Devices)·Z-0254-2026·2025-10-29

    Battery powered mobile X-ray unit recalled with water resistance reminder

    Sedecal is recalling one SM-20HF-Batt 20KW analog mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-20HF-Batt; 20KW ANALOG, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0263-2026·2025-10-29

    Four 40KW 50C X-ray systems recalled with water resistance reminder

    Sedecal is recalling four SM-40HF-B-D-C 40KW 50C mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 50C, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0255-2026·2025-10-29

    Thirty two kilowatt X-ray systems recalled with strict cleaning reminder

    Sedecal is recalling eight SM-32HF-B-D-C 32KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-32HF-B-D-C; 32KW 50G, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0285-2026·2025-10-29

    Three VIR3 mobile X-ray systems recalled with water resistance reminder

    Sedecal is recalling three SM_40HF_B_D_VIR3.004 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    SM_40HF_B_D_VIR3.004, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0266-2026·2025-10-29

    Mobile X-ray system recalled with reminder that unit is not waterproof

    Sedecal is recalling one SM-40HF-B-D-C 40KW 55C/60C mobile X-ray system after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 55C/60C, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0279-2026·2025-10-29

    Six 40KW mobile X-ray systems recalled with cleaning instruction reminder

    Sedecal is recalling six SM-40HF-B-D-C 40KW.005 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW.005, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0034-2026·2025-10-29

    Olopatadine eye drops recalled after unspecified impurity exceeded specification limit

    USV Private Limited is recalling 8,952 bottles of Olopatadine Hydrochloride Ophthalmic Solution USP 0.1% after an unspecified impurity exceeded the specification limit.

    Product
    Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 %, 5 mL (0.17 FL OZ) bottles, Manufactured for: SOLA PHARMACEUTICALS LLC, Baton Rouge, LA 70810, NDC 70512-0520-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0261-2026·2025-10-29

    Battery analog 40KW X-ray systems recalled with water resistance reminder

    Sedecal is recalling nine SM-40HF-Batt 40KW analog mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-Batt; 40KW ANALOG, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0277-2026·2025-10-29

    One hundred forty two 40KW X-ray systems recalled with cleaning reminder

    Sedecal is recalling 142 SM-40HF-B-D-C 40KW mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0258-2026·2025-10-29

    Thirty nine 40KW 50G X-ray systems recalled with cleaning reminder

    Sedecal is recalling 39 SM-40HF-B-D-C 40KW 50G mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Model Number SM-40HF-B-D-C; 40KW 50G, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0031-2026·2025-10-29

    Gabapentin blister packs recalled after unknown impurity exceeded specification

    The Harvard Drug Group is recalling Gabapentin Capsules USP 100 mg in 10-capsule blister packs after routine stability testing returned an out-of-specification result for highest unknown impurity.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0273-2026·2025-10-29

    Mobile X-ray systems recalled with cleaning reminder over water resistance limits

    Sedecal is recalling 10 mobile X-ray systems after emailing consignees to remind users that the equipment is not water-resistant and must be cleaned strictly per the manual.

    Product
    Model Number SM-40HF-B-D-C; 40KW 70C READY, Mobile X-ray system
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0242-2026·2025-10-29

    Digital diagnostic X-ray systems recalled with reminder about improper cleaning

    Sedecal is recalling 56 SM-40HF-B-D-KM (AeroDR X30) mobile digital diagnostic X-ray systems after emailing consignees to remind users that the equipment is not water-resistant.

    Product
    Sedecal Mobile Digital Diagnostic X-Ray Systems; SM-40HF-B-D-KM (AeroDR X30)
    Category
    Medical Device
    Distribution
    3 states