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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 67248

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
September 11, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
ArjoHuntleigh Inc.

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

1 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 1

The Rotoprone therapy System is an advanced patient care system for the treatment and prevention of pulmonary complications. The Rotoprone Therapy System provides up to 62 degrees in both prone and supine positions as well as Trendelenburg/Reverse Trendelenburg positioning. Product Usage: Use of the Rotoprone Therapy System is indicated for patients with severe acute respiratory distress syndrome (ARDS). These are critical patients who are at higher risk of cardiac arrest and mortality. Placing a patient in the prone position may reopen collapsed airways and thus improve pulmonary gas exchange and respiratory mechanics.

Z-0926-2014
Recall number
Z-0926-2014
Initiated
September 11, 2013
Classification
Class II
Status
Terminated
Recalling firm
ArjoHuntleigh Inc.
Quantity
231 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The lock pin can become stuck in the "in" position during the manual rotation, resulting in the inability to prone a patient

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

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Inspect official wording and provenance

Reason for recall

The lock pin can become stuck in the "in" position during the manual rotation, resulting in the inability to prone a patient

Code information

Model #209500

Distribution pattern

US Nationwide and Middle East