Juzo Soft 2081ATFFSH00 IRecalls & reported problems
Julius Zorn, Inc. · 20-30 mmHg, Soft, Elastic Panty, FF,Short, Trend, I · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00640095246312), received between Aug 20, 2024 and Jan 27, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Loss of Osseointegration” (2 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.
Reports received per month
Most reported problems
Device problems
- Loss of Osseointegration2
Patient problems
- Failure of Implant2
- Inflammation1
- Osteolysis1
- Unspecified Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 27, 2026Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Inflammation; Unspecified Infection
MAUDE report 24190886 ↗InjuryAug 20, 2024Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Osteolysis
MAUDE report 20006592 ↗
Other STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES) devices
- Juzo Soft 2081ATFFSH00 IIIJulius Zorn, Inc. · STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES)10 reports
- Juzo Soft 2081ATFFSH00 IIJulius Zorn, Inc. · STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES)1 report
- Juzo Dynamic 3511AGFFSBSH00 IVJulius Zorn, Inc. · STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES)1 report
- Juzo Dynamic 3511AD5SB IVJulius Zorn, Inc. · STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES)1 report
- Juzo Dynamic 3511MXADFF5SB00 VJulius Zorn, Inc. · STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES)1 report
- SOLIDEA 065234Calzificio Pinelli Srl · Stocking, Medical Support (For General Medical Purposes)1 report
- GOGO® 24332Knit-Rite, Inc · Stocking, Medical Support (For General Medical Purposes)1 report
- Juzo Dynamic 3511AGFFSBSH00 IJulius Zorn, Inc. · STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES)1 report
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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