Device recall
Z-0149-2026: BioPro Endo Head (Metal uni-polar, 38-55) Product Number/Description 10179 ENDO…
FDA device recall · Class II · BioPro, Inc.
Key facts
| Recall number (Z-number) | Z-0149-2026 |
|---|---|
| Recall event | 97605 |
| Product | BioPro Endo Head (Metal uni-polar, 38-55) Product Number/Description 10179 ENDO MD 38 10180 ENDO MD 41 10181 ENDO MD 43 10182 ENDO MD 45 10183 ENDO MD 47 10184 ENDO MD 49 10185 ENDO MD 51 10186 ENDO MD 53 10187 ENDO MD 55 10188 ENDO SH 38 10189 ENDO SH 41 10190 ENDO SH 43 10191 ENDO SH 45 10192 ENDO… |
| Product code | LPH |
| Recalling firm | BioPro, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K895886 |
| FEI number | 1832656 |
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