BIORAPTOR/ULTRABRAID 72200774Recalls & reported problems
Smith & Nephew, Inc. · BIORAPTOR 2.9 WITH 1 ULTRABRAID · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03596010585950), received between Aug 31, 2017 and Jan 12, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (1 report).
40 other recalls cover devices cleared under the same FDA submission (K151105); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Break1
- Device Operates Differently Than Expected1
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 12, 2018Device Operates Differently Than Expected
IT WAS REPORTED THAT DURING A SHOULDER SUPERIOR LABRUM REPAIR ONE SUTURE WAS PASSED THROUGH THE LABRUM AND THE OTHER ONE WAS HELD AND THIS SUTURE WAS LEAVED FROM THE ANCHOR FOR AN UNKNOWN REASON. ANCHOR WAS NOT REMOVED AND AN ADDITIONAL HOLE WAS MADE TO COMPLETE THE PROCEDURE, NO SIGNIFICANT DELAY OR PATIENT INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7186930 ↗MalfunctionAug 31, 2017Break
IT WAS REPORTED THAT THE SCREW WAS BROKEN DURING INSERTION. ALL PIECES OF THE SCREW WERE REMOVED FROM THE PATIENT. A BACKUP DEVICE WAS AVAILABLE TO COMPLETE THE PROCEDURE FOLLOWING A SHORT DELAY. NO PATIENT IMPACT WAS REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6836626 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K151105. One submission often covers many models, so check the product and lot details in each record.
- Z-0138-2021 · Sep 9, 2020 · Open, ClassifiedTWINFIX 5.0MM AB SUTURE ANCHOR-Absorbable Suture anchors Product Number: 7210711
- Z-0171-2021 · Sep 9, 2020 · Open, ClassifiedHEALICOIL RG SA 5.5MM W/3 UB-BL CB BL BK- Absorbable Suture anchor Product Number: 72203707
- Z-0173-2021 · Sep 9, 2020 · Open, ClassifiedHEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BL- Absorbable Suture anchor Product Number: 72203801
- Z-0155-2021 · Sep 9, 2020 · Open, ClassifiedTWINFIX ULTRA 5.5MM PLLA/HA 2 UBWHT/BL--Absorbable Suture anchor Product Number: 72202602
- Z-0137-2021 · Sep 9, 2020 · Open, ClassifiedTWINFIX 5.0MM AB SUTURE ANCHOR WITH TWO- Absorbable Suture anchors Product Number: 7210710
- Z-0142-2021 · Sep 9, 2020 · Open, ClassifiedTWINFIX AB 5.0 SUTR ANCHR W/2 38 DURAB-Absorbable Suture anchors Product Number: 72200785
- Z-0141-2021 · Sep 9, 2020 · Open, ClassifiedTWINFIX AB 5.0 SUTR ANCHR W/2 38 ULTRA-Absorbable Suture anchors Product Number:72200777
- Z-0165-2021 · Sep 9, 2020 · Open, ClassifiedOSTEORAPTOR CRVD 2.3 SA UB COBRD BLUE- Absorbable Suture anchor Product Number: 72203290
- Z-0169-2021 · Sep 9, 2020 · Open, ClassifiedHEALICOIL RSB SA 4.75MM W/1 UT & 1 UB BK-- Absorbable Suture anchor Product Number: 72203705
- Z-0163-2021 · Sep 9, 2020 · Open, ClassifiedTWINFIX ULTRA HA 5.5 W/2 UB BLUE & BLK- Absorbable Suture anchor Product Number: 72202626
- Z-0146-2021 · Sep 9, 2020 · Open, ClassifiedBIORAPTOR 2.9MM SUTURE ANCHOR-Absorbable Suture anchor Product Number: 72201702
- Z-0152-2021 · Sep 9, 2020 · Open, ClassifiedOSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE -Absorbable Suture anchor Product Number: 72201995
- Z-0162-2021 · Sep 9, 2020 · Open, ClassifiedTWINFIX ULTRA HA 4.5 W/2 UB BLUE & BLK- Absorbable Suture anchor Product Number: 72202624
- Z-0157-2021 · Sep 9, 2020 · Open, ClassifiedTWINFIX ULTRA 6.5MM PLLA/HA 2 UBWHT/BL-Absorbable Suture anchor Product Number: 72202608
- Z-0151-2021 · Sep 9, 2020 · Open, ClassifiedOSTEORAPTOR 2.9 W/ 1 UB COBRAID BLUE -Absorbable Suture anchor Product Number: 72201994
…and 25 more.
Other Screw, fixation, bone devices
- NA 03.043.029Synthes GmbH · Screw, fixation, bone503 reports
- OSTEORAPTOR 72201995Smith & Nephew, Inc. · Screw, fixation, bone253 reports
- Control 360 SK12Treace Medical Concepts, Inc. · Screw, Fixation, Bone195 reports
- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-225Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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