Device recall
Z-0424-05: Bio Med Devices Patient Breathing Circuit Catalog Number: 80015 Labeled in part…
FDA device recall · Class I · Bio-Med Devices, Inc.
Key facts
| Recall number (Z-number) | Z-0424-05 |
|---|---|
| Recall event | 30580 |
| Product | Bio Med Devices Patient Breathing Circuit Catalog Number: 80015 Labeled in part: DO NOT REUSE DISPOSABLE DISPOSABLE PATIENT BREATHING CIRCUIT =-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-=-= CONTENTS: 1-PATIENT SMOOTH BORE HOSE 1-ADAPTER 22mmx22mm 22mmIDx72'' w/CLIPS 1-ADULT PRESSURE TEE w/.140 HOLE 1-LINE… |
| 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