Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754
Reported: February 14, 2024 Initiated: December 12, 2023 #Z-0983-2024
Product Description
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.
Details
- Recalling Firm
- Steris Corporation
- Units Affected
- 2
- 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.
- Location
- Mentor, OH
Frequently Asked Questions
What product was recalled? ▼
Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754. Recalled by Steris Corporation. Units affected: 2.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 14, 2024. Severity: Moderate. Recall number: Z-0983-2024.
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