CLASS II ONGOING Device recall · Reported 22 Jan 2025 · FDA Enforcement Report
Behavioral Health Hospital bed side rails recalled
NOA Medical Industries is recalling Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX, distributed in California, Georgia, Massachusetts, Michigan. The recall was initiated on 5 Nov 2024 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0838-2025
- FDA event ID
- 95971
- Recalling firm
- NOA Medical Industries, Washington, MO
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 5 Nov 2024
- FDA classified
- 10 Jan 2025
- Reported
- 22 Jan 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Device Malfunction
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 5 Nov 2024 | Recall initiated by company | |
| 10 Jan 2025 | Classified by FDA | +66 days |
| 22 Jan 2025 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX
Where it was distributed
US: GA, MI. MA, CA
Questions about this recall
Why was it recalled?
Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.
Which lots are affected?
UDI/DI 00817492012745, Serial Numbers: 2038043534, 2038042756, 2038042755, 2038042750, 2038042751, 2038042752, 2038042753, 2038042754, 2038042757, 2038042244, 2038041722, 2038038738, 2038038750, 2038038749, 2038038748, 2038038747, 2038038746, 2038038745, 2038038744, 2038038758, 2038038757, 2038038756, 2038038754, 2038038753, 2038038752, 2038038755, 2038038743, 2038038742, 2038038737, 2038038751, 2038038739, 2038038740, 2038038741, 2038038766.
Where was it sold?
US: GA, MI. MA, CA
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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