Smith & Nephew, Inc. Endoscopy Division
37 recalls on record · Latest: Jul 23, 2014
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Agency notice ledger
Federal filing book Smith & Nephew, Inc. Endosc… MID-BOOK · SINGLE-AGENCY
#462 of 14,151 · 37 notices · 0.035% archive
- BOOK 37 notices
- RANK #462 of 14,151
- SHARE 0.035% archive
- AGENCY FDA Devices (37)
- CAT medical devices
- CATS 1 category
- LATEST Jul 23, 2014
- PHOTO Abbott Vascular
Nearest notice-volume peer: Abbott Vascular (0 notice gap)
Smith & Nephew, Inc. Endoscopy Division accounts for about 0.035% of the 104,423-notice archive on 37 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →
Where Smith & Nephew, Inc. Endosc… sits among 14,151 recalling firms
Smith & Nephew, Inc. Endoscopy Division ranks 462nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Smith & Nephew, Inc. Endosc… vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
37 462nd of 14151 higher than 13,687 of 14,151 firms
Firms, banded by distinct federal recall-event inventory
Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13
Smith & Nephew, Inc. Endosc… in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Smith & Nephe… (this)
Smith & Nephew, Inc. Endoscopy Division
37 notices
- Abbott Vascul…
Abbott Vascular
37 notices
- Bimbo Bakerie…
Bimbo Bakeries USA
37 notices
- BioPro, Inc.
BioPro, Inc.
37 notices
- Burlington Me…
Burlington Medical, LLC
37 notices
- Direct Rx
Direct Rx
37 notices
What this shows Smith & Nephew, Inc. Endoscopy Division holds about 0.035% of archive notices alongside 37 distinct filings.
FDA Devices Moderate Jul 23, 2014
SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: 72203852 Fastener, fixation, nondegradable, soft tissue
FDA Devices Moderate Jul 23, 2014
SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Code: 72203853 Fastener, fixation, nondegradable, soft tissue
FDA Devices Moderate Jul 23, 2014
SUTUREFIX Ultra S Double Loaded Suture Product Code: 72203854 Fastener, fixation, nondegradable, soft tissue
FDA Devices Moderate Jul 23, 2014
SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Blue Product Code: 72203841 Fastener, fixation, nondegradable, soft tissue
FDA Devices Moderate Jul 23, 2014
SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Product Code: 72203842 Fastener, fixation, nondegradable, soft tissue
FDA Devices Moderate Sep 25, 2013
OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Black; Part Number: 72201992 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
OSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture, White; Part Number: 72202165 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
BIORAPTOR 2.9 mm Suture Anchor Straight, pack of 2 ULTRABRAID Suture; Part Number: 72200690 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black; Part Number: 72201996 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX Ultra 5.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID) with Needles; Part Number: 72202616 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Blue ; Part Number: 72201995 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
OSTEORAPTOR CURVED 2.3 mm Suture Anchor SA ULTRABRAID COBRAID Suture, Blue; Part Number: 72203290 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX" Ultra PLLA/HA 6.5 mm with 2 ULTRABRAID" Suture, White / Black: Part Number: 72202608 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Blue; Part Number: 72201994 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX ULTRA PLLA/HA 5.5 mm Suture Anchor with 3 ULTRABRAID Suture: Part Number: 72202603 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX Ultra HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture, Blue / Black; Part Number: 72202626 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX Ultra PLLA/HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black: Part Number: 72202602 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
BIORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture; Part Number: 72200774 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
BIORAPTOR 2.9 mm Suture Anchor, pack of 1 ULTRABRAID Suture: 72200689 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX Ultra PLLA/HA 6.5 mm with 3 ULTRABRAID Suture; Part Number: 72202610 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX Ultra HA 6.5 mm with 2 ULTRABRAID Suture, Blue / Black; Part Number: 72202631 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture; Part Number: 72200775 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
RAPTORMITE" 3.7 mm PLLA with two ULTRABRAID" Sutures Size 0 and Needles; Part Number: 72201805 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
BIORAPTOR 2.9 mm Suture Anchor with DURABRAID" Suture; Part Number: 72200783 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture, White / Blue; Part Number: 72202597 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture, White; Part Number: 72201991 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
OSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture, Black; Part Number: 72203291 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID) with Needles; Part Number: 72202620 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX" Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID") with Needles; Part Number: 72202612 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture, Blue; Part Number: 72201993 Biodegradable suture anchor
FDA Devices Moderate Sep 25, 2013
TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture, Blue / Black; Part Number: 72202624 Biodegradable suture anchor
FDA Devices Moderate Aug 15, 2012
Smith & Nephew 5.5 mm Dyonics Bonecutter ,Electroblade Full Radius Part Number: 7205962 Product Usage: The Dyonics Electroblade Resector is indicated for use in arthroscopic surgical procedures of large and small articular cavities. The Dyonics Electroblade Resector is effective in soft and osseous tissue resection and in hemostasis of bleeding vessels. It is intended for arthroscopic procedures using saline solution, Ringers lactate or other conductive solutions as an irrigant under dir
FDA Devices Moderate Aug 15, 2012
Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white, COBRAID- blue), sterile Part Number: 72202897 Product Usage: intended for use for the reattachment of soft tissue to bone
FDA Devices Moderate Aug 15, 2012
Smith & Nephew Dyonics Electroblade Resector, 4.5mm Full Radius Blade, BONECUTTER Part Number: 72202213 Product Usage: The Dyonics Electroblade Resector is indicated for use in arthroscopic surgical procedures of large and small articular cavities. The Dyonics Electroblade Resector is effective in soft and osseous tissue resection and in hemostasis of bleeding vessels. It is intended for arthroscopic procedures using saline solution, Ringers lactate or other conductive solutions as an irri
FDA Devices Moderate Aug 15, 2012
Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white, COBRAID-blue), sterile Part Number: 72202895 Product Usage: intended for use for the reattachment of soft tissue to bone
FDA Devices Moderate Aug 15, 2012
Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures (COBRAID-blue, COBRAIDblack), sterile Part Number: 72202896 Product Usage: intended for use for the reattachment of soft tissue to bone
FDA Devices Moderate Aug 15, 2012
Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor with two #2 ULTRABRAID sutures (blue, blue-COBRAID) with Needles Product Usage: intended for use for the reattachment of soft tissue to bone Part Number: 72202618
Smith & Nephew, Inc. Endosc… holds a measurable archive slice
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (37 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name Smith & Nephew, Inc. Endosc…? ▼
PlainRecalls indexes 37 distinct federal recall events naming Smith & Nephew, Inc. Endoscopy Division, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Smith & Nephew, Inc. Endosc… sit among other recalling firms? ▼
Smith & Nephew, Inc. Endoscopy Division ranks #462 of 14,151 by distinct recall-event count among 14,151 firms in this archive (97th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Smith & Nephew, Inc. Endosc…'s notices? ▼
FDA Devices accounts for 37 of this firm's 37 indexed notices.
What product category dominates Smith & Nephew, Inc. Endosc…'s filing book? ▼
Filings for Smith & Nephew, Inc. Endoscopy Division span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Smith & Nephew, Inc. Endoscopy Division: 37 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.
Firm-level totals aggregate distinct federal recall events naming Smith & Nephew, Inc. Endoscopy Division; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026