VERASENSE VERASENSE for Zimmer Biomet Persona CR E-F/3-11 LeftRecalls & reported problems
Orthosensor Inc · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
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.
Recalls naming this device
- Jul 12, 2018Class IITerminated
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Z-0082-2019 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other Intraoperative Orthopedic Joint Assessment Aid devices
- VERASENSE VERASENSE for Zimmer Biomet Persona CR C-D/3-9 LeftOrthosensor Inc · Intraoperative Orthopedic Joint Assessment Aid1 recall0 reports
- VERASENSE VERASENSE for Zimmer Biomet Persona CR G-H/7-12 LeftOrthosensor Inc · Intraoperative Orthopedic Joint Assessment Aid1 recall0 reports
- VERASENSE VERASENSE for Zimmer Biomet Persona CR C-D/3-9 RightOrthosensor Inc · Intraoperative Orthopedic Joint Assessment Aid1 recall0 reports
- VERASENSE VERASENSE for Zimmer Biomet Persona CR G-H/7-12 RightOrthosensor Inc · Intraoperative Orthopedic Joint Assessment Aid1 recall0 reports
- VERASENSE VERASENSE for Zimmer Biomet Persona CR E-F/3-11 RightOrthosensor Inc · Intraoperative Orthopedic Joint Assessment Aid1 recall0 reports
- VERASENSE VERASENSE for Smith & Nephew Journey II CR 5-6 RightOrthosensor Inc · Intraoperative Orthopedic Joint Assessment Aid1 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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