NOA Medical Industries Inc recalls NOA Medical Industries Behavioral Health Hospital bed side rails
Reason for recall
Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Affected products & lots
- NOA Medical Industries Behavioral Health Hospital bed side rails, Product number1055050GRY-BOX34 affected lots20380435342038042756203804275520380427502038042751203804275220380427532038042754
+26 more
20380427572038042244203804172220380387382038038750203803874920380387482038038747203803874620380387452038038744203803875820380387572038038756203803875420380387532038038752203803875520380387432038038742203803873720380387512038038739203803874020380387412038038766
What the firm is doing
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.
DistributionShow detailsHide
US: GA, MI. MA, CA
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-0838-2025
- FDA device classification · IKXOfficial FDA classification for this device type
- CFR regulation · 21 CFR 890.5050The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find NOA Medical Industries IncSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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