Class II — Micro-Tech (Nanjing) Co., Ltd.
| Recalling firm | Micro-Tech (Nanjing) Co., Ltd. |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units |
| 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 |
| Quantity | 1360 pcs |
| Distribution | US Nationwide Distribution in the states of AL, CA, IN, FL, GA, MO, MT, NV, OK, OR, PA TX & Washington D.C. |
| Initiated | 2018-09-20 |
| Classified | 2018-10-23 |
| Terminated | 2019-10-21 |
| Recall number | Z-0237-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Micro-Tech (Nanjing) Co., Ltd. (Z-0237-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/81176/
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