FDA Device recall Z-1221-2015
KimVent Closed Suction System for Adults, Double Swivel Elbow, 14 Fr. Sterile, Distributed by Kimberly Clark Global Systems, LLC
- FDA Device
- Class II
- terminated
- Published 2015-03-11
On 2015-03-11 the FDA classified a Class II recall of KimVent Closed Suction System for Adults, Double Swivel Elbow, 14 Fr. Sterile, Distributed by Kimberly Clark Global Systems, LLC by Halyard Health, citing defect: A hole or crack was found which may cause air to leak.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1221-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-16 |
| Published | 2015-03-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Halyard Health |
| Distribution | CA, FL, IL, LA, MA, MN, MS, NM, NY, OK, TX |
Product
KimVent Closed Suction System for Adults, Double Swivel Elbow, 14 Fr. Sterile, Distributed by Kimberly Clark Global Systems, LLC.
Reason
Defect: A hole or crack was found which may cause air to leak.
Identifiers
| code_info | Product Code; 22103, Lot number: M4132T614 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1221-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.