RegWardenFDA facility compliance records
Facility

HUDSON SCIENTIFIC LLC

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

Activity by year

FDA actions on record by year2018: 1 recalls; 2020: 1 inspections201712018201912020202120222023202420252026
  • Recalls (1)
  • Inspections (1)

Devices registered here (1)

  • Holding Chambers, Direct Patient Interface
    Product code NVP (opens in a new tab) · Class II · Anesthesiology · 21 CFR 868.5630

Recalls & enforcement

  • Class IITerminated2018-07-02
    The device and its accessories may not have been manufactured according to current Good Manufacturing Practices. In addition, the firm has received three complaints regarding electric shocks received when using the device.

FDA inspections (1)

  • VAI2020-02-25
    Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

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. “HUDSON SCIENTIFIC LLC (FEI 3013037032) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3013037032-hudson-scientific-llc/

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