QUICKANCHOR PANACRYL 212135Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10886705001996), received between Sep 3, 2018 and Feb 13, 2020 — classified as 4 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Crack” (4 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 16, 2026.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 13, 2020Crack; Loosening of Implant Not Related to Bone-Ingrowth; Crack; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED BY THE AFFILIATE BY CUSTOMER'S EMAIL THAT DURING AN UNKNOWN PROCEDURE THE SUTURE MATERIAL OF THE SUPER QA+ #2 PAN CP-2 EA TORN DESPITE THE EXPERIENCED PULLING AND KNOWLEDGE OF THE IMPLANT. NO PATIENT CONSEQUENCE AND NO SURGICAL DELAY WAS REPORTED. ADDITIONAL INFORMATION: ADEQUATE SUPPLY OF THE KNEE EXTENSOR WAS NOT POSSIBLE.

  Patient problems: Tissue Damage

  MAUDE report 9706548 ↗
• InjuryFeb 13, 2020Crack; Loosening of Implant Not Related to Bone-Ingrowth; Crack; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED BY THE AFFILIATE BY CUSTOMER'S EMAIL THAT DURING AN UNKNOWN PROCEDURE THE SUTURE MATERIAL OF THE SUPER QA+ #2 PAN CP-2 *EA TORN DESPITE THE EXPERIENCED PULLING AND KNOWLEDGE OF THE IMPLANT. NO PATIENT CONSEQUENCE AND NO SURGICAL DELAY WAS REPORTED. ADDITIONAL INFORMATION: ADEQUATE SUPPLY OF THE KNEE EXTENSOR WAS NOT POSSIBLE.

  Patient problems: Tissue Damage

  MAUDE report 9706048 ↗
• InjuryFeb 13, 2020Crack; Loosening of Implant Not Related to Bone-Ingrowth; Crack; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED BY THE AFFILIATE BY CUSTOMER'S EMAIL THAT DURING AN UNKNOWN PROCEDURE THE SUTURE MATERIAL OF THE SUPER QA+ #2 PAN CP-2 EA TORN DESPITE THE EXPERIENCED PULLING AND KNOWLEDGE OF THE IMPLANT. NO PATIENT CONSEQUENCE AND NO SURGICAL DELAY WAS REPORTED. ADDITIONAL INFORMATION: ADEQUATE SUPPLY OF THE KNEE EXTENSOR WAS NOT POSSIBLE.

  Patient problems: Tissue Damage

  MAUDE report 9705926 ↗
• InjuryFeb 13, 2020Crack; Loosening of Implant Not Related to Bone-Ingrowth; Crack; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED BY THE AFFILIATE BY CUSTOMER'S EMAIL THAT DURING AN UNKNOWN PROCEDURE THE SUTURE MATERIAL OF THE SUPER QA+ #2 PAN CP-2 EA TORN DESPITE THE EXPERIENCED PULLING AND KNOWLEDGE OF THE IMPLANT. NO PATIENT CONSEQUENCE AND NO SURGICAL DELAY WAS REPORTED. ADDITIONAL INFORMATION: ADEQUATE SUPPLY OF THE KNEE EXTENSOR WAS NOT POSSIBLE.

  Patient problems: Tissue Damage

  MAUDE report 9705913 ↗
• MalfunctionSep 3, 2018Material Frayed; Material Frayed

  THIS IS REPORT 2 OF 2 FOR THE SAME EVENT. IT WAS REPORTED BY THE AFFILIATE IN (B)(6) THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE, IT WAS OBSERVED THAT TWO GII SUPER QUICK ANKER PLUS SUTURE THREADS TORE AT BOTH ANCHOR DEVICES. IT IS UNKNOWN IF THERE WERE ANY DELAYS IN THE PROCEDURE NOR IS IT KNOWN WHAT THE SURGEON DID TO COMPLETE THE PROCEDURE. DEVICES HAVE BEEN DISCARDED BY THE CUSTOMER. THERE WAS PATIENT INVOLVEMENT REPORTED. THERE WERE NO INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL MEDWATCH REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7840995 ↗
• MalfunctionSep 3, 2018Material Frayed; Material Frayed

  THIS IS REPORT 1 OF 2 FOR THE SAME EVENT. IT WAS REPORTED BY THE AFFILIATE IN (B)(6) THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE, IT WAS OBSERVED THAT TWO GII SUPER QUICK ANKER PLUS SUTURE THREADS TORE AT BOTH ANCHOR DEVICES. IT IS UNKNOWN IF THERE WERE ANY DELAYS IN THE PROCEDURE NOR IS IT KNOWN WHAT THE SURGEON DID TO COMPLETE THE PROCEDURE. DEVICES HAVE BEEN DISCARDED BY THE CUSTOMER. THERE WAS PATIENT INVOLVEMENT REPORTED. THERE WERE NO INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL MEDWATCH REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7840971 ↗