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Outlook® 490564Recalls & reported problems

B. Braun Medical Inc. · OUTLOOK PUMP SET 3 CARESITE LADS 133 IN. · Class 2

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
3

Summary

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

3 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Oct 29, 2025Open, Classified

    Potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime (occlusion).

    Z-0708-2026 · Root cause: Process control · FDA record ↗

  2. Jun 17, 2024Open, Classified

    Potential for the backcheck valve to malfunction, resulting in backflow of medication from secondary (piggyback) IV containers into primary IV containers and the inability to prime, resulting in patient injuries of adverse drug reaction and/or product malfunction with loss of medication/blood.

    Z-2404-2024 · Root cause: Process control · FDA record ↗

  3. Aug 10, 2021Terminated

    Leakage of the pump set within the cassette portion of the pump sets, potential for delays in administration of medications, under-delivery or incomplete dosing and bloodstream infections.

    Z-2557-2021 · Root cause: Under Investigation by firm · FDA record ↗

Other Pump, infusion devices

All Pump, infusion devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.