Severity
Moderate
FDA Devices recall · Reported January 22, 2025
Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.
Noa Medical Industries Inc recalled NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050G… - a moderate-severity action.
NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050G… was recalled by Noa Medical Industries Inc in January 22, 2025. Reason: Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.. Check the official notice for the remedy. Verify recall #Z-0838-2025 with the FDA Devices before acting.
The recall
Noa Medical Industries Inc issued this moderate-severity FDA Devices recall-Red button used to engage side rails can break or become stuck making it difficult to engage the side rail..
Sourced from official FDA Devices enforcement records. Verify recall #Z-0838-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Devices action (record #Z-0838-2025) was formally reported on January 22, 2025, with the manufacturer initiating the action on November 5, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. Noa Medical Industries Inc is listed as the recalling firm, operating out of Washington, MO. Federal records list the affected scope as 34 units.
The documented reason for this recall is: Red button used to engage side rails can break or become stuck making it difficult to engage the side rail. Distribution data in the federal record shows the product reached: US: GA, MI. MA, CA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
34 units
Related Recalls
6
3 from same agency
NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX
Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-0838-2025 |
| Date reported | January 22, 2025 |
| Date initiated | November 5, 2024 |
| Recalling firm | Noa Medical Industries Inc |
| Firm location | Washington, MO |
| Affected scope | 34 units |
| Distribution | US: GA, MI. MA, CA |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
· 2026-07-02
· 2026-06-25
· 2026-06-18
GE Medical Systems Information Technologies Inc · 2026-06-03
Medline Industries, LP · 2026-06-03
Compare this recall with Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Ser… →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported January 22, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.