← FDA ENFORCEMENT
Z-2740-2026Class II

3B Medical, Inc.

Recalling firm
3B Medical, Inc.
Product type
Device
Status
Ongoing
Report date
2026-07-22
Distribution
US Nationwide distribution.
Firm state
OH
Product quantity
375
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

Packaging and labeling discrepancy involving product size identification and associated Unique Device Identifier (UDI/GTIN).

Product description

Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number: RII1001 (Small), RII1002 (Medium), RII1003 (Large) Software Version: N/A Product Description: Nasal pillows interface intended for use with positive airway pressure therapy devices. The device delivers airflow from a PAP device to the patient's nose and is secured using adjustable headgear. Component: No

Code / lot info

Lot Code: Affected Catalog Numbers: RII1001, RII1002, RII1003 Affected Lots RII1001: 220121 220121 220191 RII1002: 220121 220121 220191 RII1003: 220121 220121 220191

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.