RegWardenFDA facility compliance records
Facility

Jiangmen Dacheng Medical Equipment Co., Ltd.

3 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2016: 1 inspections; 2021: 2 recalls; 2026: 1 recalls12016201720182019202022021202220232024202512026
  • Recalls (3)
  • Inspections (1)

Devices registered here (1)

Recalls & enforcement

  • Class IIOngoing2026-07-13
    Overheating of the 115V CPU board may cause the device to shut down.
  • Class IITerminated2021-11-22
    This recall has been initiated to provide a labeling update with revised instruction how to operate the unit with Cold Therapy pads.
  • Class IITerminated2021-06-17
    There is a potential risk of device contamination and patient infection associated with the device because of the potential for organisms (including Nontuberculous mycobacteria NTM) to grow in the water systems of any heater-cooler device, and contaminated water from any heater-c…

FDA inspections (1)

  • NAI2016-05-04
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Jiangmen Dacheng Medical Equipment Co., Ltd. (FEI 3010168054) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3010168054-jiangmen-dacheng-medical-equipment-co-lt/

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