Exact FDA event identifier

Event 76934

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

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Event summary

Timeline bucket: March 22, 2017
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Smith & Nephew, 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

PERI-LOC VOLAR DISTAL RADIUS - RIGHT 3H STD HEAD LOCKING PLATE, 62 MM LENGTH, SST PLATE, REF 71823114, QTY: (1) NON-STERILE, Rx only, Smith & nephew, Inc., Memphis TN 38116

Z-2036-2017

Recall number: Z-2036-2017
Initiated: March 22, 2017
Classification: Class II
Status: Terminated
Recalling firm: Smith & Nephew, Inc.
Quantity: 12 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

This lot of left plates were laser etched and packaged as right plates.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Mixed-up of materials/components

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

This lot of left plates were laser etched and packaged as right plates.

Code information

Lot 16DM15958

Distribution pattern

Internationally to the country of : India