FDA recall Z-2379-2021

Baxter Healthcare Corporation · Class II · device

Product

Baxter prismaflex, HF 1000 PAES membrane, REF 107140 Used with Prismaflex or PrisMax control units for continuous fluid management and renal replacement therapies.

Reason for recall

Products labeled as sterile were distributed, but may not have been sterilized. Baxter confirmed Steril Milano observed nonconformances that were not reported to Baxter Data was manipulated to appear to be conforming

Distribution

US Nationwide distribution.

Key facts

Status
Terminated
Initiation date
2021-07-22
Report date
2021-09-08
Termination date
2024-01-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2379-2021