Official recall record
Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2026-03-11
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Brand on record
- Windstone Medical Packaging, Inc.
What the authority reported
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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