FDA Device recall Z-0237-2019
Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF401…
- FDA Device
- Class II
- terminated
- Published 2018-10-31
On 2018-10-31 the FDA classified a Class II recall of Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level) BF401… by Micro Tech Nanjing, citing single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0237-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-09-20 |
| Published | 2018-10-31 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Micro Tech Nanjing |
| Distribution | US |
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
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
Identifiers
| code_info | Lot Number - M180409031 Date of Manufacture - 20180409 Use By - 20220408 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0237-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.