Device recall
Z-1968-2020: BD Alaris PCEA Administration Set, Microbore Tubing with Yellow Identification…
FDA device recall · Class II · BD SWITZERLAND SARL
Key facts
| Recall number (Z-number) | Z-1968-2020 |
|---|---|
| Recall event | 85525 |
| Product | BD Alaris PCEA Administration Set, Microbore Tubing with Yellow Identification Stripe ASV, Catalog Number 10800177 - Product Usage: Microbore Tubing with Yellow Identification Stripe Anti-siphon Valve Use Aseptic Technique Set cannot be used for gravity infusion. 1. Connect PCA syringe to female… |
| Product code | FPA |
| Recalling firm | BD SWITZERLAND SARL |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 2, 2020 |
| 510(k) numbers | K811885 |
| FEI number | 3012798826 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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