Device recall
Z-2067-2019: Centurion Convenience Kits, containing BD Alaris Pump Infusion Sets. BD code…
FDA device recall · Class I · Medline Industries Inc
Key facts
| Recall number (Z-number) | Z-2067-2019 |
|---|---|
| Recall event | 82951 |
| Product | Centurion Convenience Kits, containing BD Alaris Pump Infusion Sets. BD code 11522558 (Centurion code 110931) contained inside kits DYNJ52509A and DYNJ52510A. Product Usage: The Centurion Primary Set Pack and Primary Warmer Pack Convenience Kit helps continuously or intermittently deliver fluids… |
| Recalling firm | Medline Industries Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 18, 2021 |
| FEI number | 1417592 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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