Juzo Soft 2081ATFFSH00 IIIRecalls & reported problems
Julius Zorn, Inc. · 20-30 mmHg, Soft, Elastic Panty, FF,Short, Trend, III · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 10
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 00640095246336), received between May 16, 2025 and May 7, 2026 — classified as 10 injuries.
The most frequently reported specific device problem is “Loss of Osseointegration” (8 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 Osseointegration8
- Fracture2
Patient problems
- Failure of Implant10
- Pocket Erosion3
- Inflammation1
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
InjuryMay 7, 2026Fracture
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT BREAKAGE. THE DENTAL IMPLANT WAS EXPLANTED AS A RESULT.
Patient problems: Failure of Implant
MAUDE report 25117337 ↗InjuryFeb 19, 2026Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 24386118 ↗InjuryJul 2, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Inflammation
MAUDE report 22387659 ↗InjuryJun 17, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Pocket Erosion
MAUDE report 22234945 ↗InjuryJun 17, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Pocket Erosion
MAUDE report 22234870 ↗InjuryJun 15, 2025Fracture; Fracture
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FRACTURE.
Patient problems: Failure of Implant
MAUDE report 22208700 ↗InjuryMay 22, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant; Pocket Erosion
MAUDE report 22071213 ↗InjuryMay 16, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 22039935 ↗InjuryMay 16, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 22039559 ↗InjuryMay 16, 2025Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 22039533 ↗
Other STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES) devices
- Juzo Soft 2081ATFFSH00 IJulius Zorn, Inc. · STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES)2 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.
How reports and recalls are matched · Editorial policy · Report an error on this page