EasyStand Bantam Extra SmallRecalls & reported problems
Altimate Medical Inc. · Class 2
- 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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Oct 4, 2022Terminated
Some EasyStand Bantam Small and Extra Small standers with the non-supine option may have been manufactured with a component that affects the operation of the leg assembly bracket to maintain the standers non-supine position.
Z-0243-2023 · Root cause: Pending · FDA record ↗
Other Chair, Positioning, Electric devices
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- LC358XL LC358XL/CA358XLPride Mobility Products Corp · Chair, Positioning, Electric18 reports
- LC250Pride Mobility Products Corp · Chair, Positioning, Electric12 reports
- LC358M LC358M/BC358M/CA358MPride Mobility Products Corp · Chair, Positioning, Electric1 death11 reports
- LC358S LC358S/CA358SPride Mobility Products Corp · Chair, Positioning, Electric7 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.