Recall events
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Event 76414
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
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
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1239-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[26656]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
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
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20288]
FDA event record
· Exact recall-number query on openFDA
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
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
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1240-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[15380]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
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
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[19109]
FDA event record
· Exact recall-number query on openFDA
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
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
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1241-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38490]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
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
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[24419]
FDA event record
· Exact recall-number query on openFDA
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
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
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1242-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[50838]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
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
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[23803]
FDA event record
· Exact recall-number query on openFDA
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
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
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1243-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[38492]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
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
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[20276]
FDA event record
· Exact recall-number query on openFDA
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
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
Enrichment source openFDA Device Recall
Exact join Official recall number Z-1244-2017
Source locator 0001-device-recall-0001-of-0001.json.zip#results[3788]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
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
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[19101]
FDA event record
· Exact recall-number query on openFDA