Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 76414

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

Open FDA event record

Event summary

Timeline bucket
February 02, 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

6 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 6

Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701

Z-1239-2017
Recall number
Z-1239-2017
Initiated
February 02, 2017
Classification
Class II
Status
Terminated
Recalling firm
Smith & Nephew, Inc.
Quantity
2646

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The single use devices are provided sterile and do not have an expiration date on the label.

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 single use devices are provided sterile and do not have an expiration date on the label.

Code information

Batch Numbers: 50586138 50458123 50418120 50339534 50306882 50285907 50248565 50231427 50197615 50171397 50158655 50138049 50119457 50089297 50082581 50069485

Distribution pattern

Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela

device · product 2 of 6

Smith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702

Z-1240-2017
Recall number
Z-1240-2017
Initiated
February 02, 2017
Classification
Class II
Status
Terminated
Recalling firm
Smith & Nephew, Inc.
Quantity
2496

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The single use devices are provided sterile and do not have an expiration date on the label.

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 single use devices are provided sterile and do not have an expiration date on the label.

Code information

Batch Numbers: 50525150 50386077 50261802 50197616 50178740 50171398 50158656 50138050 50121538 50103379 50089298 50082582 50061131

Distribution pattern

Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela

device · product 3 of 6

Smith & Nephew Dyonics Saw Blade, Short, Product Number 3703

Z-1241-2017
Recall number
Z-1241-2017
Initiated
February 02, 2017
Classification
Class II
Status
Terminated
Recalling firm
Smith & Nephew, Inc.
Quantity
4500

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The single use devices are provided sterile and do not have an expiration date on the label.

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 single use devices are provided sterile and do not have an expiration date on the label.

Code information

Batch Numbers: 50525150 50386077 50261802 50197616 50178740 50171398 50158656 50138050 50121538 50103379 50089298 50082582 50061131

Distribution pattern

Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela

device · product 4 of 6

Smith & Nephew Dyonics Saw Blade, Short, Narrow, Product Number 3704

Z-1242-2017
Recall number
Z-1242-2017
Initiated
February 02, 2017
Classification
Class II
Status
Terminated
Recalling firm
Smith & Nephew, Inc.
Quantity
8748

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The single use devices are provided sterile and do not have an expiration date on the label.

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 single use devices are provided sterile and do not have an expiration date on the label.

Code information

Batch Numbers: 50525150 50386077 50261802 50197616 50178740 50171398 50158656 50138050 50121538 50103379 50089298 50082582 50061131

Distribution pattern

Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela

device · product 5 of 6

Smith & Nephew Dyonics Saw Blade, Narrow, Product Number 3705

Z-1243-2017
Recall number
Z-1243-2017
Initiated
February 02, 2017
Classification
Class II
Status
Terminated
Recalling firm
Smith & Nephew, Inc.
Quantity
3462

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The single use devices are provided sterile and do not have an expiration date on the label.

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 single use devices are provided sterile and do not have an expiration date on the label.

Code information

Batch Numbers: 50525150 50386077 50261802 50197616 50178740 50171398 50158656 50138050 50121538 50103379 50089298 50082582 50061131

Distribution pattern

Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela

device · product 6 of 6

Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706

Z-1244-2017
Recall number
Z-1244-2017
Initiated
February 02, 2017
Classification
Class II
Status
Terminated
Recalling firm
Smith & Nephew, Inc.
Quantity
1410

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The single use devices are provided sterile and do not have an expiration date on the label.

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 single use devices are provided sterile and do not have an expiration date on the label.

Code information

Batch Numbers: 50439354 50393992 50252777 50208023 50171402 50138054 50103142 50066114 576304

Distribution pattern

Nationwide Foreign: Brazil, Canada, Chile , China, Denmark, Hong Kong, India, Mexico, Peru, Singapore, Venezuela