RegWardenFDA facility compliance records
Facility

TOTAL RESOURCES INT'L.

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

Activity by year

FDA actions on record by year2022: 1 recalls20172018201920202021120222023202420252026
  • Recalls (1)

Devices registered here (1)

  • First Aid Kit Without Drug
    Product code OHO (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4014

Recalls & enforcement

  • Class IITerminated2022-03-11
    ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due to a Fluid Bed Drier exhaust system breach, which presents the possibility of cross-contamination wh…

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. “TOTAL RESOURCES INT'L. (FEI 3002703161) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002703161-total-resources-int-l/

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