# FDA recall Z-0983-2024

> **Steris Corporation** · Class II · device recall initiated 2023-12-12.

## Product

Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754

## Reason for recall

Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or a procedural delay.

## Distribution

Worldwide - US Nationwide distribution in the states of AZ, CA, FL, IL, IN, IA, KS, LA, MN, MS, NV, NJ, OH, OK, OR, PA, TN, TX, UT, WA, WI & Puerto Rico, and the countries of Australia, Canada, Mexico & New Zealand.

## Key facts

- **Recall number:** Z-0983-2024
- **Recalling firm:** Steris Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-12
- **Report date:** 2024-02-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mentor, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0983-2024

## Citation

> AI Analytics. FDA recall Z-0983-2024. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-0983-2024. Source: US FDA. Licensed CC0.

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