Exact FDA event identifier

Event 76729

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

Event summary

Timeline bucket: March 09, 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

4 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 4

Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthopedic

Z-1854-2017

Recall number: Z-1854-2017
Initiated: March 09, 2017
Classification: Class II
Status: Terminated
Recalling firm: Smith & Nephew, Inc.
Quantity: 1 unit

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

labeling are incorrect

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling Change Control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.

Code information

Batch 15HM05197

Distribution pattern

Worldwide Distribution - US (Nationwide) Internationally to Colombia, Denmark, Finland, France, Great Britain, Italy, and Singapore

device · product 2 of 4

D-RAD, 1.8MM X 16MM, LOCKING PEG, QTY: (1), STERILE R, RES 74671816 Orthopedic

Z-1855-2017

Recall number: Z-1855-2017
Initiated: March 09, 2017
Classification: Class II
Status: Terminated
Recalling firm: Smith & Nephew, Inc.
Quantity: 19 units

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

labeling are incorrect

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling Change Control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.

Code information

Batch number 15KM05493

Distribution pattern

Worldwide Distribution - US (Nationwide) Internationally to Colombia, Denmark, Finland, France, Great Britain, Italy, and Singapore

device · product 3 of 4

D-RAD, 2.4MMX 20MM, S.T. CORTEX SCREW, QTY: (1), STERILE R, RES 74682420 Orthopedic

Z-1856-2017

Recall number: Z-1856-2017
Initiated: March 09, 2017
Classification: Class II
Status: Terminated
Recalling firm: Smith & Nephew, Inc.
Quantity: 100 units

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

labeling are incorrect

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling Change Control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.

Code information

Batch number 14MM07780R

Distribution pattern

Worldwide Distribution - US (Nationwide) Internationally to Colombia, Denmark, Finland, France, Great Britain, Italy, and Singapore

device · product 4 of 4

D-RAD, S.T. LOCKING SCREWS, T7, QTY: (1), STERILE R, in the following sizes: (a) 2.4MM X 10MM, RES 74692410 (b) 2.4MM X 12MM, RES 74692412 (c) 2.4MM X 16MM, RES 74692416 (d) 2.4MM X 22MM, RES 74692422 (e) 2.4MM X 24MM, RES 74692424

Z-1857-2017

Recall number: Z-1857-2017
Initiated: March 09, 2017
Classification: Class II
Status: Terminated
Recalling firm: Smith & Nephew, Inc.
Quantity: 197 units

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

labeling are incorrect

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Labeling Change Control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.

Code information

Batch numbers: (a) RES 74692410: 15GM13481, 15JM17474, 15JM17475 (b) RES 74692412: 15EM010131, 15JM07539 (c) RES 74692416: 15FM06118 (d) RES 74692422: 16AM19135 (e) RES 74692424: 15JM19559

Distribution pattern

Worldwide Distribution - US (Nationwide) Internationally to Colombia, Denmark, Finland, France, Great Britain, Italy, and Singapore