QUADROX-iD BEQ-HMOD70000-USA #SQUADROX-iD Ad./coated/ no.Fil.Recalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

2 other recalls cover devices cleared under the same FDA submission (K150267); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. May 18, 2023Class IIOpen, Classified

   1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory s sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and crushed areas. Both issues may compromise the sterile barrier of the packaging, and exposure to non-sterile product may result in inflammation, infection, sepsis, and ischemia.

   Z-1635-2023 · Root cause: Pending · Recall details · FDA record ↗

2. May 18, 2023Class IIOpen, Classified

   Product packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may result in inflammation, infection, sepsis, and ischemia.

   Z-1656-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K150267. One submission often covers many models, so check the product and lot details in each record.

• Z-1636-2023 · May 18, 2023 · Open, Classified
  BEQ-HMO 50000-USA/ QUADROX-i Small, Oxygenator used during cardiopulmonary bypass Item no. 701067905
• Z-1371-2016 · Feb 23, 2016 · Terminated
  QUADROX-i oxygenators Custom tubing packs for the oxygenator