Device recall
Z-0429-05: Bio-Med Patient Breathing Circuit Product NUmber: 3030-5 Labeled in part: ONE…
FDA device recall · Class I · Bio-Med Devices, Inc.
Key facts
| Recall number (Z-number) | Z-0429-05 |
|---|---|
| Recall event | 30580 |
| Product | Bio-Med Patient Breathing Circuit Product NUmber: 3030-5 Labeled in part: ONE SET - SINGLE USE CATALOG NO. 3030-5 PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT HOSE 22mmIDx60'' 1-PRESSURE GAGE LINE 1/8''IDx72'' 1-PATIENT HOSE 22mmIDx6'' 1-EXHALATION VALVE… |
| 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