FDA recall Z-1332-2021

Tenacore LLC · Class I · device

Product

Alaris Infusion Pump 8100 Bezel (plastic piece only), Part: TIPA-8100-4410

Reason for recall

Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The separation of one or more bezel repair part posts may result in free flow, over infusion, under infusion or interruption of infusion.

Distribution

US distribution to states of: WA, AZ, NY, TX, LA, CA, NV, ME, MN, DE, NC, FL, MO, KY, TN, and PA

Key facts

Status
Terminated
Initiation date
2021-02-25
Report date
2021-04-14
Termination date
2024-08-05
Voluntary/Mandated
Voluntary: Firm initiated
Location
Santa Ana, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1332-2021