RecallReported October 21, 2026
Class II recall by Becton Dickinson & Co.
BD Phoenix Panel NMIC-306. Catalog Number: 449292.
FDA's enforcement report of October 21, 2026 lists a Class II recall by Becton Dickinson & Co. of Sparks, MD. Product: BD Phoenix Panel NMIC-306. Catalog Number: 449292. Status: Ongoing.
On the record
- Recalling firm
- Becton Dickinson & Co.
- Location
- Sparks, MD
- Classification
- Class II
- Status
- Ongoing
- Recall number
- Z-0140-2027
- Product type
- Devices
- Recall initiated
- 2026-08-13
- Reported by FDA
- 2026-10-21
The full record
An account shows the reason for the recall, where the product was distributed and the lots.
What a recall is
FDA classifies a recall by the hazard. Class I: a reasonable probability that the product will cause serious adverse health consequences or death. Class II: the product may cause temporary or medically reversible harm, or the probability of serious harm is remote. Class III: the product is not likely to cause adverse health consequences.
More
Watch Becton Dickinson & Co
A free account shows the last 7 days of every record. Pro adds a watchlist: one email when FDA acts on a company you name.
From FDA enforcement reports. The record may have changed since it was read.
Approve Suite is not affiliated with FDA, or with Becton Dickinson & Co.
See something wrong on this page? Write to info@approvesuite.com and we will check it against the source. How corrections work.