Device recall
Z-1857-2013: List No. 14217-28; Y-TYPE BLOOD SET; 200 Micron Filter, Prepierced Y-Site…
FDA device recall · Class I · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1857-2013 |
|---|---|
| Recall event | 65689 |
| Product | List No. 14217-28; Y-TYPE BLOOD SET; 200 Micron Filter, Prepierced Y-Site, Non-Vented, 80 Inch, Non-DEHP; For Blood Product Administration; Made in Costa Rica; Product Inquiries should be directed to Hospira., Inc., Lake Forrest, IL 60045 USA Hospira Blood sets are designed for Blood Product… |
| Product code | BRZ |
| Recalling firm | Hospira Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 24, 2017 |
| 510(k) numbers | K101677 |
| 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