Medline DYNJP2414RRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10080196764860), received between Feb 12, 2026 and Feb 12, 2026 — classified as 2 injuries.

2 FDA recall records name this device's identifier, 2 still open.

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.

Recalls naming this device

1. Jan 7, 2026Open, Classified

   Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

   Z-1423-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

2. Jan 7, 2026Open, Classified

   Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

   Z-2128-2026 · Root cause: Process control · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 12, 2026Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY, MEDLINE DRAPES WERE RECALLED AND HAD BEEN USED DURING A TOTAL KNEE ARTHROPLASTY PROCEDURE PRIOR TO THE FACILITY BECOMING AWARE OF THE RECALL.

  Patient problems: Post Operative Wound Infection

  MAUDE report 24328086 ↗
• InjuryFeb 12, 2026Appropriate Device Problem Term/Code Not Available

  ACCORDING TO THE FACILITY, MEDLINE DRAPES WERE RECALLED AND HAD BEEN USED DURING A TOTAL KNEE ARTHROPLASTY PROCEDURE PRIOR TO THE FACILITY BECOMING AWARE OF THE RECALL. THE PROCEDURE WAS INITIALLY PERFORMED ON (B)(6) 2025. THE PATIENT SUBSEQUENTLY REQUIRED A SECOND SURGERY ON (B)(6) 2026, DUE TO AN INFECTED KNEE. THE FACILITY STATED THEY DOUBT THE INFECTIONS WERE RELATED TO THE DRAPES OR GOWNS USED.

  Patient problems: Post Operative Wound Infection

  MAUDE report 24327399 ↗