RegWardenFDA facility compliance records
Facility

Research Instruments Ltd

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

Activity by year

FDA actions on record by year2016: 1 recalls120162017201820192020202120222023202420252026
  • Recalls (1)

Devices registered here (1)

  • Accessory, Assisted Reproduction
    Product code MQG (opens in a new tab) · Class II · Obstetrics/Gynecology · 21 CFR 884.6120

Recalls & enforcement

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. “Research Instruments Ltd (FEI 3003751666) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003751666-research-instruments-ltd/

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