FDA recall Z-0768-2021

Baxter Healthcare Corporation · Class II · device

Product

MiniCap Extended Life PD Transfer Set

Reason for recall

Potential for no-flow and leaks under the twist clamp.

Distribution

Worldwide and US (Nationwide), Canada, Brazil, Mexico, Bermuda, and Indonesia

Key facts

Status
Terminated
Initiation date
2020-11-10
Report date
2021-01-13
Termination date
2023-03-24
Voluntary/Mandated
Voluntary: Firm initiated
Location
Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0768-2021