Device recall
Z-2533-2020: RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code…
FDA device recall · Class II · TELEFLEX MEDICAL INC
Key facts
| Recall number (Z-number) | Z-2533-2020 |
|---|---|
| Recall event | 85786 |
| Product | RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code 102004-000040 b) I.D. mm 5,0, Product Code 102004-000050 c) I.D. mm 6,0, Product Code 102004-000060 d) I.D. mm 7,0, Product Code 102004-000070 e) I.D. mm 8,0, Product Code 102004-000080 Product Usage: Tracheal intubation… |
| Product code | BTR |
| Recalling firm | TELEFLEX MEDICAL INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 17, 2025 |
| 510(k) numbers | K935842 |
| FEI number | 3005747797 |
At a glance
- 1–9 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