Device recall
Z-0427-05: Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A-9 Labeled in…
FDA device recall · Class I · Bio-Med Devices, Inc.
Key facts
| Recall number (Z-number) | Z-0427-05 |
|---|---|
| Recall event | 30580 |
| Product | Bio Med Devices Patient Breathing Circuit Catalog Number: 8002A-9 Labeled in part: ONE SET - SINGLE USE CATALOG NO. 8002A-9 PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx60'' 1-EXHALATION VALVE LINE 1/8''IDx108'' 1-PATIENT HOSE 22mmIDx36'' 1-PATIENT… |
| 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