Exact FDA event identifier

Event 69058

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

Event summary

Timeline bucket: July 30, 2014
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Wright Medical Technology, 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

9 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 9

CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM, REF 40S20020, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Z-2599-2014

Recall number: Z-2599-2014
Initiated: July 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Wright Medical Technology, Inc.
Quantity: 0

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Plates manufactured from an incorrect raw material.

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

Plates manufactured from an incorrect raw material.

Code information

Lot Number: 1543488

Distribution pattern

Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.

device · product 2 of 9

CLAW 3.5mm PLATE CHARLOTTE F&A SYSTEM, SIZE 30mm, 2 HOLE, USE WITH 3.5mm CLAW SCREW, REF 4013-0130, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Z-2600-2014

Recall number: Z-2600-2014
Initiated: July 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Wright Medical Technology, Inc.
Quantity: 9 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Plates manufactured from an incorrect raw material.

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

Plates manufactured from an incorrect raw material.

Code information

Lot Number: 1509955

Distribution pattern

Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.

device · product 3 of 9

CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 15mm, REF 40240215, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Z-2601-2014

Recall number: Z-2601-2014
Initiated: July 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Wright Medical Technology, Inc.
Quantity: 497 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Plates manufactured from an incorrect raw material.

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

Plates manufactured from an incorrect raw material.

Code information

Lot Numbers: 1487673, 1487674, 1487675, 1487676, 1490003, 1512150, 1512151, 1519497, 1519498, 1522019, 1522020, 1523747, 1523748, 1537072, 1537073, 1537162, 1539399, 1541615, 1541616, 1543148, 1543149

Distribution pattern

Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.

device · product 4 of 9

CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 20mm, REF 40240220, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Z-2602-2014

Recall number: Z-2602-2014
Initiated: July 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Wright Medical Technology, Inc.
Quantity: 1127 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Plates manufactured from an incorrect raw material.

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

Plates manufactured from an incorrect raw material.

Code information

Lot Numbers: 1490004, 1490005, 1490199, 1490200, 1490201, 1490202, 1518483, 1519493, 1519494, 1519495, 1522021, 1522898, 1522899, 1522900, 1523735, 1523736, 1526519, 1526520, 1526521, 1538760, 1538761, 1539402, 1540715, 1540716, 1540717, 1542703, 1542704, 1542776, 1543491, 1543891

Distribution pattern

Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.

device · product 5 of 9

CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 25mm, REF 40240225, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Z-2603-2014

Recall number: Z-2603-2014
Initiated: July 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Wright Medical Technology, Inc.
Quantity: 400 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Plates manufactured from an incorrect raw material.

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

Plates manufactured from an incorrect raw material.

Code information

Lot Numbers: 1490367, 1490368, 1512152, 1521232, 1523734, 1523746, 1537160, 1537161, 1539401, 1541613, 1541614, 1542652, 1542774, 1542775

Distribution pattern

Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.

device · product 6 of 9

CLAW II 2 HOLE PLATE ORTHOLOC 3DSi, LENGTH 30mm, REF 40240230, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Z-2604-2014

Recall number: Z-2604-2014
Initiated: July 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Wright Medical Technology, Inc.
Quantity: 178 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Plates manufactured from an incorrect raw material.

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

Plates manufactured from an incorrect raw material.

Code information

Lot Numbers: 1487670, 1487671, 1487672, 1512149, 1519496, 1523745, 1534796, 1537159, 1539400, 1540714

Distribution pattern

Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.

device · product 7 of 9

CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 20mm x 20mm, REF 40242020, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Z-2605-2014

Recall number: Z-2605-2014
Initiated: July 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Wright Medical Technology, Inc.
Quantity: 66 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Plates manufactured from an incorrect raw material.

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

Plates manufactured from an incorrect raw material.

Code information

Lot Numbers: 1512153, 1518480, 1532497, 1538075, 1538076, 1538332

Distribution pattern

Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.

device · product 8 of 9

CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 25mm x 25mm, REF 40242525, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Z-2607-2014

Recall number: Z-2607-2014
Initiated: July 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Wright Medical Technology, Inc.
Quantity: 18 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Plates manufactured from an incorrect raw material.

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

Plates manufactured from an incorrect raw material.

Code information

Lot Numbers: 1517327, 1538333, 1543490

Distribution pattern

Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.

device · product 9 of 9

CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 20mm x 25mm, REF 40242025, 1 EACH, Rx ONLY, NON STERILE Orthopedic

Z-2608-2014

Recall number: Z-2608-2014
Initiated: July 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Wright Medical Technology, Inc.
Quantity: 50 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Plates manufactured from an incorrect raw material.

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

Plates manufactured from an incorrect raw material.

Code information

Lot Numbers: 1513144, 1518479, 1534798, 1538331, 1543489

Distribution pattern

Worldwide Distribution - USA (Nationwide) and Internationally to Canada Australia, Great Britain, Germany, Spain, Netherlands, France.