Device recall
Z-1237-03: Infant reusable blood pressure cuffs, one tube, male slip luer connector, P/N…
FDA device recall · Class III · GE Medical Systems Information Technologies
Key facts
| Recall number (Z-number) | Z-1237-03 |
|---|---|
| Recall event | 26287 |
| Product | Infant reusable blood pressure cuffs, one tube, male slip luer connector, P/N 2930 , manufactured for Welch Allyn Protocol, Inc. and labeled in part: '***Reusable Blood Pressure Cuffs Infant 50 Cuffs REF 008-0625-00 PROTOCOL SYSTEMS, INC. Beaverton, OR 97008-7107 USA Assembled in Mexico***.' |
| Recalling firm | GE Medical Systems Information Technologies |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 15, 2008 |
| FEI number | 1030184 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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