KimVent Wet Pak — Class II medical device recall Z-1222-2015
Terminated recall by Halyard Health, reported 2015-03-11, distributed in CA, FL, IL, LA, MA, MN, MS, NM…. Defect: A hole or crack was found which may cause air to leak.
| Recall number | Z-1222-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Halyard Health, Roswell, GA, United States |
| Recall initiated | 2015-01-16 |
| Classified | 2015-02-27 |
| Reported by FDA | 2015-03-11 |
| Terminated | 2015-07-07 |
| Distributed | CA, FL, IL, LA, MA, MN, MS, NM, NY, OK, TX |
| Countries outside the US | JP |
| Reason classes | packaging |
| Lot numbers | AB4195U14, AB4216U06, AB4230U16, M4132T643 |
Product
KimVent Wet Pak, Closed Suction System for Adults, Double Swivel Elbow, 14 Fr. Sterile, Distributed by Kimberly Clark Global Systems, LLC.
Reason for recall
Defect: A hole or crack was found which may cause air to leak.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1222-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.