Device recall
Z-1333-04: Welch Allyn Vital Signs Monitor 5300 Series 300 Part numbers 007-0098-00 through…
FDA device recall · Class II · Welch Allyn Protocol, Inc
Key facts
| Recall number (Z-number) | Z-1333-04 |
|---|---|
| Recall event | 29233 |
| Product | Welch Allyn Vital Signs Monitor 5300 Series 300 Part numbers 007-0098-00 through 007-0159-00 |
| Product code | DQA |
| Recalling firm | Welch Allyn Protocol, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2006 |
| FEI number | 3023750 |
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