Data Foundry

Medical device recalls 2024

BEQ-HLS 7050 USA — Class II medical device recall Z-1077-2024

Ongoing recall by Maquet Medical Systems USA, reported 2024-02-21, distributed nationwide. The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconfo

Recall numberZ-1077-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMaquet Medical Systems USA, Wayne, NJ, United States
Recall initiated2024-01-16
Classified2024-02-13
Reported by FDA2024-02-21
DistributedNationwide (US)
Reason classessterility, packaging
UPC / GTIN / UDI-DI04058863080383
Lot numbers3000280906, 3000280907, 3000280908, 3000280909, 3000282253, 3000282254, 3000282255, 3000291127, 3000300688, 3000314506, 3000316206, 3000316600, 3000317531, 3000317532, 3000318850, 3000318851, 3000318852, 3000318853, 3000319748, 3000319749, 3000319750, 3000319751, 3000319778, 3000319781, 3000323082, 3000323084, 3000323085, 3000324495, 3000324496, 3000324497, 3000324499, 3000325557, 3000325558, 3000325559, 3000327120, 3000327121, 3000328404, 3000328405, 3000330091, 3000330092 and 42 more
Model numbers70106.9078

Product

BEQ-HLS 7050 USA, HLS Set Advanced 7.0, Product Code/Part Number 70106.9078. Used with the CARDIOHELP heart-lung machine.

Reason for recall

The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis, or infection.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1077-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.