FDA recall Z-1765-2022

Maquet Medical Systems USA · Class II · device

Product

BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70105.2797. A preconnected set used for extracorporeal respiratory and/or cardiovascular support, as part of the CARDIOHELP System.

Reason for recall

The firm has expanded the recall for the HLS Set Advanced regarding a potential breach in the sterility barrier that may result in compromised product sterility (prior recall was initiated November 6, 2020).

Distribution

Worldwide distribution - US Nationwide and the countries Canada and Australia.

Key facts

Status
Ongoing
Initiation date
2022-07-22
Report date
2022-09-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Wayne, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1765-2022