Device recall
Z-0135-06: LifeShield Latex-Free HEMA Y-Type Blood PlumSet, Nonvented, 122 inch, with 210…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-0135-06 |
|---|---|
| Recall event | 33659 |
| Product | LifeShield Latex-Free HEMA Y-Type Blood PlumSet, Nonvented, 122 inch, with 210 Micron Filter, Inline Dual Channel Cassette, 2 Clave Ports and Option-Lok for use with Plum Series Infusers; Hospira, Inc., Lake Forest, IL 60045 USA, Made in Costa Rica; list 12259-02 |
| Product code | BRZ |
| Recalling firm | Hospira Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 29, 2007 |
| 510(k) numbers | K830014, K865060, K920736, K941214 |
| FEI number | 3013319212 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database