# FDA recall Z-0948-2022

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-02-25.

## Product

Baxter DISCPAC Syringe Tip  Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.

## Reason for recall

Product is mislabeled as self-righting Luer slip tip caps, yellow.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of FL, GA, IL, IN, MO, PA, TX, and VA.  The countries of Canada, Austria, Germany, Netherlands, Qatar, Saudi Arabia, and Spain.

## Key facts

- **Recall number:** Z-0948-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-02-25
- **Report date:** 2022-04-27
- **Termination date:** 2026-03-02

- **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-0948-2022

## Citation

> MORVS. FDA recall Z-0948-2022. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-0948-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
