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Recall Observatory FDA recall evidence

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.

Z-1765-2022

July 22, 2022

Class II

Product summary

Firm
Maquet Medical Systems USA
Event
Event 90740
Status
Ongoing
Classification
Class II
Quantity
206 US; 48,960 Worldwide
Official record key
device-enforcement:Z-1765-2022

Official wording

Reason: 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).

Code information: UDI-DI: 04037691773513 Lot 3000183908

Distribution pattern: Worldwide distribution - US Nationwide and the countries Canada and Australia.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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).