RegWardenFDA facility compliance records
Facility

MERCEDES MEDICAL LLC

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

Activity by year

FDA actions on record by year2021: 1 recalls20172018201920201202120222023202420252026
  • Recalls (1)

Devices registered here (3)

  • Needle, Hypodermic, Single Lumen
    Product code FMI (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5570
  • Tubes, Vials, Systems, Serum Separators, Blood Collection
    Product code JKA (opens in a new tab) · Class II · Clinical Chemistry · 21 CFR 862.1675
  • Syringe, Piston
    Product code FMF (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5860

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. “MERCEDES MEDICAL LLC (FEI 1000442352) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000442352-mercedes-medical-llc/

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