HomeMedical Device recalls
Medium severity

Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateMarch 11, 2026
ReportedApril 29, 2026
Recalling firmWindstone Medical Packaging, Inc.
Country / regionUnited States MT

Hazard

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).

Affected products

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