# FDA recall Z-1973-2026

> **AVID Medical, Inc.** · Class I · device recall initiated 2026-03-13.

## Product

Halyard CATH LAB kit. Model Number: SACL75AM.

## Reason for recall

Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

## Distribution

US distribution to FL, IL, MO, MS, NC, NE, TX.

## Key facts

- **Recall number:** Z-1973-2026
- **Recalling firm:** AVID Medical, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-13
- **Report date:** 2026-05-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Toano, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1973-2026

## Citation

> AI Analytics. FDA recall Z-1973-2026. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1973-2026. Source: US FDA. Licensed CC0.

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