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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93733

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
December 12, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Steris Corporation

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

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

Z-0983-2024
Recall number
Z-0983-2024
Initiated
December 12, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Steris Corporation
Quantity
2

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

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.

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.

device · product 2 of 2

Dual Articulating Headrest, Velcro P/N P141210813, REF BF753

Z-0984-2024
Recall number
Z-0984-2024
Initiated
December 12, 2023
Classification
Class II
Status
Ongoing
Recalling firm
Steris Corporation
Quantity
80

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

UDI-DI: 00724995195885, 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.