Z-0237-2019 Class II Terminated
FDA device recall Z-0237-2019 was initiated by Micro-Tech (Nanjing) Co., Ltd. on Sep 20, 2018 and is designated Class II. Reason for recall: Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units The recall status is terminated (terminated Oct 21, 2019). Affected quantity: 1360 pcs.
Recall Details
- Product Type
- Devices
- Report Date
- Oct 31, 2018
- Initiation Date
- Sep 20, 2018
- Termination Date
- Oct 21, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1360 pcs
Product Description
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
Distribution Pattern
US Nationwide Distribution in the states of AL, CA, IN, FL, GA, MO, MT, NV, OK, OR, PA TX & Washington D.C.
Code Information
Lot Number - M180409031 Date of Manufacture - 20180409 Use By - 20220408
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0237-2019
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026