Micro-Tech (Nanjing) Co Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm, REF Catalog No recall — FDA Z-0237-2019
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
Overview of recall records associated with Micro-Tech (Nanjing) Co., Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 3.
Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
The combination of the firmness of the mass, the potential endoscope and elevator position combined with the force required to penetrate the mass may contribute to the breakage of the…
The combination of the firmness of the mass, the potential endoscope and elevator position combined with the force required to penetrate the mass may contribute to the breakage of the…
This page summarizes recall records in which the official source identifies Micro-Tech (Nanjing) Co., Ltd. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.