Device recall
Z-1367-2018: Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b)…
FDA device recall · Class II · Teleflex Medical Europe Ltd
Key facts
| Recall number (Z-number) | Z-1367-2018 |
|---|---|
| Recall event | 79579 |
| Product | Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b) 153000005 153000005 (c) 153000010 153000010 (d) 153000020 153000020 (e) 153000030 153000030 (f) 153000050 153000050 (g) 210700050 2107050 (h) 210700102 2107102 (I) 210700202 2107202 (j) 210700302 2107302 (k) 210700402… |
| Product code | BTC |
| Recalling firm | Teleflex Medical Europe Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2020 |
| FEI number | 3007134520 |
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