Micro-Tech (Nanjing) Co., Ltd.: Medical Device Recall in 2018 - (Recall #: Z-0237-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

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

Product Classification:

Class II

Date Initiated: September 20, 2018

Date Posted: October 31, 2018

Recall Number: Z-0237-2019

Event ID: 81176

Reason for Recall:

Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units

Status: Terminated

Product Quantity: 1360 pcs

Code Information:

Lot Number - M180409031 Date of Manufacture - 20180409 Use By - 20220408

Distribution Pattern:

US Nationwide Distribution in the states of AL, CA, IN, FL, GA, MO, MT, NV, OK, OR, PA TX & Washington D.C.

Voluntary or Mandated:

Voluntary: Firm initiated