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FDA Medical Device Recalls (openFDA)

NOA Medical Industries Inc: NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX

Recall number
Z-0838-2025
Recalling firm
NOA Medical Industries Inc
Product
NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX
Status
Open, Classified
Initiated
2024-11-05
Posted
2025-01-10
Terminated
not on file
Reason
Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.
Root cause
Device Design
Action
NOA Medical Industries issued an URGENT: VOLUNTARY MEDICAL DEVICE CORRECTION notice to its consignees on 11/05/2024 via email. The notice explained the problem with the device, potential risk, and temporary actions to employ to minimize the hazard until a replacement frame is installed. A replacement side rail will be provided. For questions or concerns, contact: support@noamedical.com (email), https://www.noamedical.com/ (website) or 1-636-239-7600 (telephone), Monday-Friday 7:00AM to 3:30PM, CT.
Quantity
34 units
Distribution
US: GA, MI. MA, CA
Lot, serial or model codes
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.
510(k) numbers
not on file
PMA numbers
not on file
Product code
IKX
Firm FEI
1000118429
Firm city
Washington
Firm state
MO
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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