Device recall
Z-0237-2019: Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No…
FDA device recall · Class II · Micro-Tech (Nanjing) Co., Ltd.
Key facts
| Recall number (Z-number) | Z-0237-2019 |
|---|---|
| Recall event | 81176 |
| Product | Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF40182 (Carton box level) - BF40183(Over shipper level), STERILE |
| Product code | GEN |
| Recalling firm | Micro-Tech (Nanjing) Co., Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 21, 2019 |
| FEI number | 3004837686 |
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