Device recall
Z-0845-04: Suction Instrument with Tubing, Catalog No. 305. Instrument: Yankauer without…
FDA device recall · Class II · Busse Hospital Disposables
Key facts
| Recall number (Z-number) | Z-0845-04 |
|---|---|
| Recall event | 28815 |
| Product | Suction Instrument with Tubing, Catalog No. 305. Instrument: Yankauer without Vent. *Tubing: 10'' x 1/4'' I.D. Non-Conductive. Sterile, Single Use, Latex Free. Rx ONLY. busse Hospital Disposables Hauppauge, NY 11788. --- Classification Name: Unit, Suction Operatory. Class I device, 510 (k) exempt… |
| Product code | EBR |
| Recalling firm | Busse Hospital Disposables |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 18, 2005 |
| FEI number | 2433012 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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