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Alaris, SmartSite 11613191Recalls & reported problems

BD Switzerland Sàrl · Pump Infusion Burette Set, 0.2 Micron Filter, Ball Valve, Port (Burette), 2 Y-Sites 327 cm (130 in) · Class 2

All models of Alaris, SmartSite (160)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

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.

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. Sep 11, 2025Class IOpen, Classified

    Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.

    Z-0035-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  2. Oct 11, 2023Class IIOpen, Classified

    Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).

    Z-0349-2024 · Root cause: Error in labeling · Recall details · FDA record ↗

Other Set, administration, intravascular devices

All Set, administration, intravascular devices →

Sources and updates

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