RegWardenFDA facility compliance records
Facility

MEDICEL AG

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

Activity by year

FDA actions on record by year2013: 1 recalls1’13’14’15’16’17’18’19’20’21’22’23’24’25’26
  • Recalls (1)

Devices registered here (1)

  • Folders And Injectors, Intraocular Lens (Iol)
    Product code MSS (opens in a new tab) · Class I · Ophthalmic · 21 CFR 886.4300

Recalls & enforcement

  • Class IITerminated2013-08-05
    The firm initiated this recall of one lot (121402) of nanoPOINT Injectors after they noticed that Tyvek lids might have been damaged and, therefore, the stability of the sterile barrier might be negatively affected.

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. “MEDICEL AG (FEI 1000581837) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000581837-medicel-ag/

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