Device recall
Z-0914-03: LifeShield Latex-Free 150 mL Burette Set, Nonvented, 117 Inch with Prepierced…
FDA device recall · Class III · Abbott Laboratories HPD/ADD
Key facts
| Recall number (Z-number) | Z-0914-03 |
|---|---|
| Recall event | 26343 |
| Product | LifeShield Latex-Free 150 mL Burette Set, Nonvented, 117 Inch with Prepierced Injection Site, Backcheck Valve, 2 CLAVE Ports and Removable 4-Way High Flow Stopcock Microdrip Soluset; Product 19292; Made in Costa Rica, Abbott Laboratories, North Chicago, IL 60064 |
| Product code | FPA |
| Recalling firm | Abbott Laboratories HPD/ADD |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 20, 2003 |
| 510(k) numbers | K791930 |
| FEI number | 1415939 |
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