Micro-Tech (Nanjing) Co., Ltd. recalls Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(C…

Recall date

September 20, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0237-2019

FDA classification

Class II

Brand / firm

Micro-Tech (Nanjing) Co., Ltd.

Sold / distributed

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

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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