Steris Corporation: Medical Device Recall in 2024 - (Recall #: Z-0983-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 12, 2023

Date Posted: February 14, 2024

Recall Number: Z-0983-2024

Event ID: 93733

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.

Status: Ongoing

Product Quantity: 2

Code Information:

UDI-DI: 00724995197643, date of manufacture 2023-08-14 thru 2023-10-26.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated