QUICKANCHOR ORTHOCORD 212035Recalls & reported problems

Summary

The FDA's MAUDE database contains 43 adverse event reports that list this exact device (DI 10886705001835), received between May 31, 2018 and Sep 3, 2026 — classified as 8 injuries, 35 malfunctions.

The most frequently reported specific device problem is “Break” (11 reports).

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

Recent adverse event reports

The 25 most recent of 43 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 3, 2026Detachment of Device or Device Component

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50595758 ↗
• MalfunctionFeb 24, 2026Device-Device Incompatibility

  IT WAS REPORTED BY SALES REP THAT DURING AN UNSPECIFIED PROCEDURE, THE SURGEON HAD A HARD TIME SLIDING THE HANDLE OF THE MINI QA+ #2/O OCORD V-5, WHICH CONSEQUENTLY PULLED THE NEEDLE OFF. HE HAD TO OPEN ANOTHER ANCHOR. THERE WERE NO PATIENT CONSEQUENCES OR PATIENT TREATMENT DELAY REPORTED. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2026.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24433413 ↗
• MalfunctionDec 12, 2025Product Quality Problem; Product Quality Problem

  IT WAS REPORTED THAT DURING SERVICE AND EVALUATION, IT WAS DETERMINED THAT THE SMALL BATTERY DRIVE DEVICE FUTURE WAS DAMAGED - CUT/BROKEN AND WAS MISSING COMPONENTS. IT WAS REPORTED IN THE SERVICE ORDER THAT DURING A SURGICAL PROCEDURE, WHEN OPENING THE CONTAINER, IT WAS FOUND THAT IT DID NOT INCLUDE THE PUNCH OR THE 2.0 BIT, TRIED TO REPLACE THE INSTRUMENT USING A NEEDLE, BUT DID NOT GET THE EXPECTED RESULT, SO FINALLY DECIDED NOT TO USE THE ANCHOR OR OPEN THE BIT. THERE WERE NO REPORTS OF DELAYS TO A SURGICAL PROCEDURE. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23794588 ↗
• MalfunctionSep 16, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE, WHEN THE MINI QA+ #2/O OCORD V-5 DEVICE WAS REMOVED FROM THE PACKAGING, IT WAS OBSERVED THAT THE HANDLE WAS DETACHED FROM THE INSERTER. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS A SLIGHT UNSPECIFIED DELAY IN THE PROCEDURE REPORTED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23060740 ↗
• InjuryMay 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THIS IS REPORT 1 OF 2 OF (B)(4). IT WAS REPORTED THAT ABOUT FOUR MONTHS AFTER A TEMPOROMANDIBULAR JOINT (TMJ) CORRECTION. SURGICAL PROCEDURE, THE PATIENT'S BODY STARTED TO REJECT THE 2X MINI QA+ #2/O OCORD V-5 DEVICES THAT HAD BEEN PLACED POSSIBLY DUE TO A NITINOL ALLERGY. THERE WERE REPORTS OF DELAYS IN A SURGICAL PROCEDURE REPORTED. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN (B)(6) 2024. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Foreign Body Reaction

  MAUDE report 21977573 ↗
• InjuryMay 7, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THIS IS REPORT 2 OF 2 OF (B)(4). IT WAS REPORTED THAT ABOUT FOUR MONTHS AFTER A TEMPOROMANDIBULAR JOINT (TMJ) CORRECTION. SURGICAL PROCEDURE, THE PATIENT'S BODY STARTED TO REJECT THE 2X MINI QA+ #2/O OCORD V-5 DEVICES THAT HAD BEEN PLACED POSSIBLY DUE TO A NITINOL ALLERGY. THERE WERE REPORTS OF DELAYS IN A SURGICAL PROCEDURE REPORTED. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN (B)(6) 2024. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Foreign Body Reaction

  MAUDE report 21977569 ↗
• MalfunctionMar 21, 2025Break; Break

  IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE THE MINI QA+ #2/O OCORD V-5 DEVICE ANCHOR WAS BROKEN, REMOVED ALL THE BROKEN PARTS. ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21665784 ↗
• MalfunctionFeb 11, 2025Break; Device Damaged Prior to Use; Device-Device Incompatibility; Material Deformation; Break; Device Damaged Prior to Use; Device-Device Incompatibility; Material Deformation

  IT WAS REPORTED THAT THE DURING PRE-SURGERY FOR AN UNKNOWN PROCEDURE, IT WAS OBSERVED WHEN OPENING THE PACKING THAT THE MINI QA+ #2/O OCORD V-5 DEVICE ANCHOR WAS DETACHED FROM THE SHAFT IN THE PACKAGE AND COULD NOT BE ASSEMBLED. DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE ONE OF THE DEVICES ARCS WAS MISSING AND THE INSERTER TIP WAS DEFORMED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21353651 ↗
• MalfunctionAug 15, 2024Difficult to Advance; Difficult to Advance

  IT WAS REPORTED BY THE SALES REP IN HUNGARY THAT DURING A TEMPOROMANDIBULAR JOINT RECONSTRUCTION PROCEDURE SURGICAL PROCEDURE ON (B)(6) 2024 THE MINI QA+ #2/O OCORD V-5 DEVICE, ONCE A POND DRILLING AND INCURSION, THE ANCHOR DID NOT INSERT ALL THE WAY. THE DOCTOR TRIED TO KEEP THE HANDLE ATTACHED TO THE ANCHOR THEN THE SUTURE WAS CUT. THE DOCTOR REMOVED THE ANCHOR AND RE-DRILLED AND INSERTED A NEW ANCHOR. THE CASE WAS COMPLETED WITH NO CONSEQUENCES. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19993437 ↗
• MalfunctionAug 6, 2024Migration; Migration

  REPORT 2 OF 2 FOR (B)(4). IT WAS REPORTED BY THE HEALTHCARE PROFESSIONAL IN FRANCE THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE ON (B)(6) 2024, IT WAS OBSERVED THAT WHILE USING THE MINI QA+ #2/O OCORD V-5 DEVICE, THE NEEDLE PULLED OFF THE THREAD DURING USE. IT WAS REPORTED THAT THIS PROBLEM OCCURRED ON TWO ANCHORS IN THE SAME BATCH AND THE ANCHORS WERE STILL ABLE TO BE LAID. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19916109 ↗
• MalfunctionAug 6, 2024Migration; Migration

  REPORT 1 OF 2 FOR (B)(4). IT WAS REPORTED BY THE HEALTHCARE PROFESSIONAL IN FRANCE THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE ON (B)(6) 2024, IT WAS OBSERVED THAT WHILE USING THE MINI QA+ #2/O OCORD V-5 DEVICE, THE NEEDLE PULLED OFF THE THREAD DURING USE. IT WAS REPORTED THAT THIS PROBLEM OCCURRED ON TWO ANCHORS IN THE SAME BATCH AND THE ANCHORS WERE STILL ABLE TO BE LAID. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19916092 ↗
• MalfunctionAug 5, 2024Break; Break

  IT WAS REPORTED BY AN EMPLOYEE THAT DURING A TEMPOROMANDIBULAR JOINT SURGICAL PROCEDURE ON (B)(6) 2024 THE MINI QA+ #2/O OCORD V-5 DEVICE NEEDLE WITH BIT WAS BROKEN UPON INSERTION. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19907785 ↗
• MalfunctionJan 25, 2024Break; Break

  IT WAS REPORTED BY SALES REP THAT DURING A WRIST LIGAMENT REPAIR ON (B)(6) 2024, IT WAS OBSERVED THAT THE MINI QA+ W/ #2/0 OCORD AND V-5 NEEDLE W/BIT DEVICE HAS SUTURE IMPLANT BROKEN. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18580378 ↗
• MalfunctionNov 15, 2023Break; Break

  IT WAS REPORTED BY THE HEALTHCARE PROFESSIONAL IN CHINA THAT DURING AN ANKLE RECONSTRUCTION PROCEDURE ON 10/1/2023, IT WAS OBSERVED THAT THE ANCHOR ON THE MINI QA+ #2/O OCORD V-5 DEVICE WAS BROKEN OFF, THEN REMOVED ALL THE BROKEN PARTS. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18142902 ↗
• MalfunctionNov 12, 2023Break; Break

  IT WAS REPORTED BY A HEALTHCARE PROFESSIONAL IN NEW ZEALAND THAT DURING AN UNKNOWN PROCEDURE ON AN UNKNOWN DATE, IT WAS OBSERVED THAT THE MINI QA+ W/ #2/0 OCORD AND V-5 NEEDLE W/BIT DEVICE BROKE INTO THE BONE WHEN MALLETED. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18117335 ↗
• MalfunctionJun 14, 2023Difficult to Advance; Migration; Difficult to Advance; Migration

  IT WAS REPORTED BY THE SALES REP IN HONG KONG THAT DURING AN UNKNOWN PROCEDURE ON (B)(6)2023, IT WAS OBSERVED THAT THE MINI QA+ W/ #2/0 OCORD AND V-5 NEEDLE W/BIT DEVICE PULLED OUT AND WAS NOT ABLE TO BE IMPLANTED IN THE PATIENT. IT WAS UNKNOWN IF AND HOW THE PROCEDURE WAS COMPLETED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17131139 ↗
• InjurySep 20, 2022Migration; Migration

  IT WAS REPORTED BY SALES REP THAT DURING AN UNKNOWN PROCEDURE ON (B)(6) 2022, A MINI QA+ W/ #2/0 OCORD AND V-5 NEEDLE W/BIT DEVICE WAS USED. IT WAS REPORTED THAT POSTOPERATIVELY ON (B)(6) 2022, IT WAS OBSERVED THAT THE DEVICE WAS "ERODING OUT OF THE PATIENT¿S SKIN¿. ACCORDING TO THE REPORT, THE PATIENT RECEIVED A PROCEDURE IN CLINIC ON (B)(6) 2022 WHERE THE PHYSICIAN ASSISTANT USED A SUTURE REMOVAL KIT TO CUT OUT THE PROTRUDING VISIBLE SUTURE ANCHOR MATERIAL LEAVING A PINHOLE WHICH SHE COVERED WITH OINTMENT. IT WAS REPORTED THAT THEY DID NOT GET AN IMAGING OR USE THE C-ARM IN CLINIC. IT WAS REPORTED THAT THE PATIENT HAS A FOLLOW UP APPOINTMENT WITH THEIR PHYSICIAN THE FOLLOWING WEEK BUT THE EXACT DATE AND TIME HAS NOT BEEN CONFIRMED YET. IT WAS REPORTED THAT THE PATIENT HAS ¿SOME REDNESS AROUND THE DORSAL 3RD OF THE PHALANX. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Unspecified Tissue Injury

  MAUDE report 15456222 ↗
• MalfunctionSep 9, 2022Migration; Migration

  IT WAS REPORTED BY THE SALES REP THAT DURING A SCAPHOID REPAIR PROCEDURE ON 8/24/22, IT WAS OBSERVED THAT ONE OF THE TINES ON THE ANCHOR ON THE MINI QA+ W/ #2/0 OCORD AND V-5 NEEDLE W/BIT DEVICE DID NOT DEPLOY SO THE ANCHOR PULLED OUT. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15391758 ↗
• MalfunctionSep 7, 2022Migration; Migration

  IT WAS REPORTED BY SALES REP THAT DURING AN UNKNOWN PROCEDURE ON (B)(6) 2022, IT WAS OBSERVED THAT A MINI QA+ W/ #2/0 OCORD AND V-5 NEEDLE W/BIT INITIALLY PULLED OUT DURING THE FIRST ATTEMPT AT SETTING THE ANCHOR WHEN IT WAS INSERTED INTO THE 5TH DISTAL PHALANX TO REATTACHED THE EXTENSOR TENDON. ACCORDING TO THE REPORT, AFTER PULLING OUT THE FIRST TIME, THE ANCHOR WAS RESET ONTO THE INSERTER, THE BONE WAS DRILLED AGAIN AND THE ANCHOR WAS INSERTED AND SET SUCCESSFULLY WITHIN THE BONE AND THE SURGEON CONFIRMED THAT FIXATION WAS ACHIEVED RADIOGRAPHICALLY. THE REPAIR WAS COMPLETED ON A SECOND ATTEMPT AFTER THE ANCHOR. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Unspecified Tissue Injury

  MAUDE report 15372240 ↗
• MalfunctionJan 26, 2022Unintended Movement; Unintended Movement

  IT WAS REPORTED BY THE SALES REP THAT DURING A HAND SURGERY ON (B)(6) 2022, IT WAS OBSERVED THAT THE SUTURES ON THE MINI QA+ #2/O OCORD V-5 DEVICE WERE LOOSE. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13358519 ↗
• MalfunctionJan 11, 2022Break; Break

  IT WAS REPORTED BY THE CUSTOMER IN CHINA THAT DURING AN ANTERIOR CRUCIATE LIGAMENT RECONSTRUCTION SURGERY ON (B)(6) 2022, IT WAS OBSERVED THAT THE MINI QA+ #2/O OCORD V-5 ANCHOR DEVICE BROKE OFF. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13227824 ↗
• MalfunctionNov 15, 2021Break; Break

  IT WAS REPORTED BY THE SALES REP THAT DURING AN UNKNOWN PROCEDURE ON (B)(6) 2021, IT WAS OBSERVED THAT THE DISTAL TIP ON THE MINI QA+ W/ #2/0 OCORD AND V-5 NEEDLE W/BIT DEVICE BROKE UPON INSERTION DUE TO HARD BONE. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12816360 ↗
• MalfunctionOct 15, 2021Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED BY THE SALES REP THAT DURING A MALLET FINGER PROCEDURE ON (B)(6) 2021, IT WAS OBSERVED THAT THE MINI QA+ #2/O OCORD V-5 ANCHOR DEVICE DID NOT DEPLOY. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12641385 ↗
• MalfunctionSep 2, 2020Migration or Expulsion of Device; Migration or Expulsion of Device

  IT WAS REPORTED THAT DURING THE SURGERY OF LATERAL MALLEOLAR LIGAMENT REPAIR, WHEN REMOVED THE SHAFT, NOTED THE ANCHOR WAS ALSO PULLED OUT. ANOTHER DEVICE WAS USED TO COMPLETE THE SURGERY. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. NO ADDITIONAL INFORMATION COULD BE PROVIDED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10482623 ↗
• MalfunctionSep 2, 2020Migration or Expulsion of Device; Migration or Expulsion of Device

  IT WAS REPORTED THAT DURING THE SURGERY OF LATERAL MALLEOLAR LIGAMENT REPAIR , WHEN REMOVED THE SHAFT, NOTED THE ANCHOR WAS ALSO PULLED OUT. ANOTHER DEVICE WAS USED TO COMPLETE THE SURGERY. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. NO ADDITIONAL INFORMATION COULD BE PROVIDED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10482304 ↗