RecallReported September 23, 2026
Class I recall by BD SWITZERLAND SARL
BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3 Smar…
FDA's enforcement report of September 23, 2026 lists a Class I recall by BD SWITZERLAND SARL of Eysins, N/A. Product: BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3 Smar…. Status: Ongoing.
On the record
- Recalling firm
- BD SWITZERLAND SARL
- Location
- Eysins, N/A
- Classification
- Class I
- Status
- Ongoing
- Recall number
- Z-3080-2026
- Product type
- Devices
- Recall initiated
- 2026-08-19
- Reported by FDA
- 2026-09-23
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.
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From FDA enforcement reports. The record may have changed since it was read.
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