RegWardenFDA facility compliance records
Company

Micro-Tech (Nanjing) Co., Ltd.

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

Recalls by year

FDA actions on record by year2018: 2 recalls20172201820192020202120222023202420252026
  • Recalls (2)

Registered facilities (3)

Recalls & enforcement

  • Class IITerminated2018-09-20
    Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
  • Class IITerminated2018-03-12
    The combination of the firmness of the mass, the potential endoscope and elevator position combined with the force required to penetrate the mass may contribute to the breakage of the needle in the human body, which could cause injury.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “Micro-Tech (Nanjing) Co., Ltd. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9067602-micro-tech-nanjing-co-ltd/

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