# FDA recall Z-1576-2022

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-07-22.

## Product

Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Orange: a) 25 pack, REF H93867025, b) 100 pack, REF H93867100

## Reason for recall

There is a potential of the packaging not maintaining a sterile barrier for the tip caps.

## Distribution

Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.

## Key facts

- **Recall number:** Z-1576-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-22
- **Report date:** 2022-08-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1576-2022

## Citation

> AI Analytics. FDA recall Z-1576-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1576-2022. Source: US FDA. Licensed CC0.

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