Exact FDA event identifier

Event 65062

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

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Event summary

Timeline bucket: March 12, 2013
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Berchtold Corp.

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

Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables

Z-1488-2013

Recall number: Z-1488-2013
Initiated: March 12, 2013
Classification: Class II
Status: Terminated
Recalling firm: Berchtold Corp.
Quantity: 3763

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

The firm received complaints for unintended movements.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The firm received complaints for unintended movements.

Code information

The hand controls are neither serialized nor lot coded.

Distribution pattern

Nationwide Distribution