Device recall
Z-0425-05: Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A Labeled in part…
FDA device recall · Class I · Bio-Med Devices, Inc.
Key facts
| Recall number (Z-number) | Z-0425-05 |
|---|---|
| Recall event | 30580 |
| Product | Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A Labeled in part: ONE SET - SINGLE USE CATALOG NO. 8002A PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx42'' 1-PRESSURE GAGE LINE 1-PATIENT HOSE 22mmIDx6'' 1-EXHALATION VALVE w/HOLDING ARM&… |
| Product code | CBK |
| Recalling firm | Bio-Med Devices, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 21, 2005 |
| FEI number | 3003952420 |
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