Class III — Kimberly-Clark Corporation
| Recalling firm | KIMBERLY-CLARK CORPORATION |
|---|---|
| Registered facility | KIMBERLY-CLARK PERU S.R.L. - Santa Clara Mill (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | The impacted product was not intended for commercial distribution to end users. |
| Product | ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File. The Kimberly-Clark ULTRA Fabric Reinforced Surgical Gown is a sterile, single use surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fluids, and particulate material. |
| Quantity | 32 cases |
| Distribution | US (nationwide) including the states of CA, CO, LA, NM, OK, TX and WA. |
| Initiated | 2010-12-31 |
| Classified | 2012-09-20 |
| Terminated | 2012-11-01 |
| Recall number | Z-2425-2012 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Kimberly-Clark Corporation (Z-2425-2012).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/62577/
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