# FDA recall Z-1920-2026

> **Windstone Medical Packaging, Inc.** · Class II · device recall initiated 2026-03-11.

## Product

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

## 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).

## Distribution

US Nationwide distribution in the states of GA, OR, TN, and WA.

## Key facts

- **Recall number:** Z-1920-2026
- **Recalling firm:** Windstone Medical Packaging, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-11
- **Report date:** 2026-04-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Billings, MT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1920-2026

## Citation

> AI Analytics. FDA recall Z-1920-2026. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1920-2026. Source: US FDA. Licensed CC0.

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