FDA recall Z-1050-2021

Product

K-201 GUIDE SHEATH KIT 2.0MM, model no. K-201 - Product Usage: Used with endoscopes to collect cells or tissue specimens in the respiratory organs.

Reason for recall

Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used.

Distribution

US Nationwide distribution.

Key facts

Status

Terminated

Initiation date

2021-01-04

Report date

2021-02-17

Termination date

2024-03-11

Voluntary/Mandated

Voluntary: Firm initiated

Location

Kuroishi, N/A, Japan

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1050-2021