Health o meter Professional 498KLRecalls & reported problems
Pelstar, LLC · Digital Scale · Class 1
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
- Oct 7, 2011Terminated
There is a potential for an electrical short when installing or replacing the batteries in the remote display head of the scales. This short may cause the batteries to smoke, burn or burst.
Z-0294-2012 · Root cause: Device Design · Recall details · FDA record ↗
Other Scale, Stand-On, Patient devices
- seca 284seca GmbH & Co. KG · Scale, Stand-On, Patient1 report
- Welch Allyn, Inc. 901110Welch Allyn, Inc. · SCALE, STAND-ON, PATIENT1 report
- Welch Allyn, Inc. 901109Welch Allyn, Inc. · SCALE, STAND-ON, PATIENT1 report
- Welch Allyn, Inc. 901109Welch Allyn, Inc. · SCALE, STAND-ON, PATIENT1 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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