FDA recall record

3B Medical, Inc. Ultrasoft Oxygen Cannula, 12 Foot Model / recall — FDA Z-0828-2025

The devices were inadvertently shipped after their expiration date.

Class IIclassification
Z-0828-2025official record ID
Jan 15, 2025report date

Recall record at a glance

Official recordZ-0828-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firm3B Medical, Inc.
Report dateJan 15, 2025
Recall initiation dateNov 27, 2024
Quantity5010 units
LocationWinter Haven, FL, United States

Official product description

Brand Name: 3B Medical, Inc. Product Name: Ultrasoft Oxygen Cannula, 12 Foot Model / Catalog Number: O2U2012 Lot Number: 20170403 Product Description: Nasal Cannulas for use with Oxygen Concentrators

Why the product was recalled

The devices were inadvertently shipped after their expiration date.

Distribution information

US: Massachusetts and Arkansas OUS: None

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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