Device recall
Z-0503-06: AquaPak Sterile Water for Inhalation, USP, 760 mL blow-molded plastic bottle for…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0503-06 |
|---|---|
| Recall event | 34120 |
| Product | AquaPak Sterile Water for Inhalation, USP, 760 mL blow-molded plastic bottle for use with a respiratory gas humidifier; 10 bottles per case; manufactured by Hudson Respiratory Care, Inc., Temecula, CA 92589-9020 USA; catalog #037-00 |
| Product code | BTT |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 11, 2006 |
| FEI number | 3004959265 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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