FDA recall Z-0166-2018

Abbott Laboratories, Inc · Class II · device

Product

Tubing, Peristaltic Head Part Number 7-35009685-01 for use in clinical chemistry systems.

Reason for recall

The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000 has the possibility to leak due to a manufacturing issue associated with the tubing connector.

Distribution

Worldwide distribution to US, Canada, France, and Germany.

Key facts

Status
Completed
Initiation date
2017-09-29
Report date
2017-11-29
Voluntary/Mandated
Voluntary: Firm initiated
Location
Irving, TX, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0166-2018