BIOKNOTLESS PANACRYL ETHIBOND 212739Recalls & reported problems
Depuy Mitek, LLC · BIOKNOTLESS RC Anchor w/PANACRYL PLA Absorbable Anchor, Size 1 (4 metric) PANACRYL braided absorbable suture anchor loop, Size 2/0 green ETHIBOND braided polyester suture utility loop. · Class 2 · Implant
All models of BIOKNOTLESS PANACRYL ETHIBOND (3)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886705002245), received between Mar 23, 2021 and Mar 23, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (1 report).
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
- Migration1
Patient problems
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 23, 2021Migration; Migration
THIS FILE IS A REVIEW OF THE FOLLOWING JOURNAL ARTICLE: JIMÉNEZ-MARTÍN, A., ET AL (2013) SLAP LESIONS: CLINICAL EXPERIENCE OF 63 CASES. SA ORTHOPAEDIC JOURNAL, VOL. 12, PAGES 32-37 (SPAIN). THE STUDY EMPHASIZES ON THE REVIEW OF THE SUPERIOR LABRUM ANTERIOR AND POSTERIOR INJURIES OR SLAP INJURIES AND TO VALUE CLINICAL AND WORKING FINAL RESULTS AFTER ITS TREATMENT. THE PATIENTS EVALUATED ON COURSE OF THIS STUDY: 63 PATIENTS. THE ARTICLE DESCRIBES THE FOLLOWING PROCEDURE: SHOULDER REPAIR THE DEVICES INVOLVED WERE: UNKNOWN BIOKNOTLESS ANCHOR COMPLICATIONS DESCRIBED: WE OBSERVED THAT IMPLANTS MOVED IN 15.2% OF CASES. SEVEN CASES REQUIRED A SECOND OPERATION.
Patient problems: Unspecified Tissue Injury
MAUDE report 11553307 ↗
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- Speed Shift SE-2020-10Synthes GmbH · Staple, Fixation, Bone1 recall10 reports
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- LUPINE ORTHOCORD 210709Depuy Mitek, LLC · STAPLE, FIXATION, BONE56 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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