Single-Use Biopsy Forceps — Class II medical device recall Z-0237-2019
Terminated recall by Micro-Tech (Nanjing) Co., Ltd., reported 2018-10-31, distributed nationwide. Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
| Recall number | Z-0237-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Micro-Tech (Nanjing) Co., Ltd., Nanjing, N/A, China |
| Recall initiated | 2018-09-20 |
| Classified | 2018-10-23 |
| Reported by FDA | 2018-10-31 |
| Terminated | 2019-10-21 |
| Distributed | Nationwide (US) |
| Quantity | 1,360 units |
| Lot numbers | M180409031 |
| Model numbers | BF40180, NBF13-01130230 |
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
Reason for recall
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0237-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.