Device recall
Z-0752-04: NEONATE 3 DISPOSABLE BLOOD PRESSURE CUFF WITH 1 TUBE, a disposable 1 piece cuff…
FDA device recall · Class II · Welch Allyn Inc
Key facts
| Recall number (Z-number) | Z-0752-04 |
|---|---|
| Recall event | 28428 |
| Product | NEONATE 3 DISPOSABLE BLOOD PRESSURE CUFF WITH 1 TUBE, a disposable 1 piece cuff for single patient use only. Sold under the Welch Allyn ''Tycos'' label with Part # 5082-103-1 and sold as part of a multi-pack (1 of each size) with Part #5082-241-9 - Welch Allyn Inc., Skaneateles Falls, NY; Allegiance… |
| Product code | DXQ |
| Recalling firm | Welch Allyn Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 1, 2005 |
| FEI number | 1316463 |
At a glance
- None Linked 510(k)s
- 10–99 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