← FDA ENFORCEMENT
Z-1920-2026Class II

Windstone Medical Packaging, Inc.

Recalling firm
Windstone Medical Packaging, Inc.
Product type
Device
Status
Ongoing
Report date
2026-04-29
Distribution
US Nationwide distribution in the states of GA, OR, TN, and WA.
Firm state
MT
Product quantity
380 units
Initiated by
Voluntary: Firm initiated
Reason for recall

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).

Product description

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

Code / lot info

UDI-DI: B098AMS149940; Lot Numbers: 220039 221423 224226 224793 225009

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.