Zimmer Biomet™ 89-8521-470-30Recalls & reported problems
Zimmer Surgical SA · Class 1
All models of Zimmer Biomet (17)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024581739), received between Nov 29, 2023 and Nov 29, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Battery Problem” (1 report).
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
- Battery Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 29, 2023Battery Problem; Battery Problem
IT WAS REPORTED THAT THE BATTERY WAS SHOWING AN ERROR CODE. IT DID NOT PROVIDE POWER DUE TO THE BATTERY'S STATE OF HEALTH AND ALSO DUE TO OVERHEATING. THIS EVENT IS RELATED TO AN OVERHEATING MALFUNCTION THAT COULD POTENTIALLY LEAD TO A SERIOUS INJURY. HOWEVER, NO PATIENT HARM OR FURTHER OUTCOME WAS REPORTED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18233942 ↗
Other Battery, Replacement, Rechargeable devices
- NA 05.001.202Synthes GmbH · BATTERY, REPLACEMENT, RECHARGEABLE263 reports
- Zimmer Biomet™ 89-8521-470-40Zimmer Surgical SA · Battery, Replacement, Rechargeable228 reports
- Zimmer Biomet™ 89-8510-440-10Zimmer Surgical SA · Battery, Replacement, Rechargeable90 reports
- Zimmer Biomet™ 89-8521-470-20Zimmer Surgical SA · Battery, Replacement, Rechargeable34 reports
- NA 05.001.204Synthes GmbH · BATTERY, REPLACEMENT, RECHARGEABLE22 reports
- NA 05.001.231Synthes GmbH · BATTERY, REPLACEMENT, RECHARGEABLE21 reports
- NA 05.001.227Synthes GmbH · BATTERY, REPLACEMENT, RECHARGEABLE11 reports
- Zimmer Biomet™ 89-8510-440-20Zimmer Surgical SA · Battery, Replacement, Rechargeable8 reports
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