FDA Device recall Z-2060-2016
*** 1) Product labeled in part: List No. 14220-28
- FDA Device
- Class II
- terminated
- Published 2016-07-06
On 2016-07-06 the FDA classified a Class II recall of *** 1) Product labeled in part: List No. 14220-28 by Hospira, citing intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV administration sets.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2060-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-09 |
| Published | 2016-07-06 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Hospira |
| Distribution | US |
Product
*** 1) Product labeled in part: List No. 14220-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, CLAVE Y-Site, Non-Vented, 110 Inch, Non-DEHP; Product Usage: The CLAVE of the secondary port is used as an easy secondary access that allows concurrent and piggyback mode in infusion. It is normally used with a syringe or a secondary IV infusion set.
Reason
Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV administration sets.
Identifiers
| code_info | ***** CANADA DISTRIBUTION ***** *** 1) List Number 14220-28-01 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2060-2016%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.