FDA recall Z-1408-2022

Product

Nonsterile convenience kit: regard Item #830014016, LD00199P - C Section Mother.

Reason for recall

Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.

Distribution

Distribution was made to MO. There was no foreign/military/government distribution.

Key facts

Status

Terminated

Initiation date

2022-06-03

Report date

2022-07-27

Termination date

2023-04-14

Voluntary/Mandated

Voluntary: Firm initiated

Location

Republic, MO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1408-2022