RecallReported September 30, 2026
Class II recall by Philips North America Llc
Ingenia Ambition S and Ingenia Ambition X; Model Numbers (REF): 1. 781359 (S), 2. 782108 (S), 3. 782139 (S), 4. 781356 (X), 5. 782109 (X), 6…
FDA's enforcement report of September 30, 2026 lists a Class II recall by Philips North America Llc of Cambridge, MA. Product: Ingenia Ambition S and Ingenia Ambition X; Model Numbers (REF): 1. 781359 (S), 2. 782108 (S), 3. 782139 (S), 4. 781356 (X), 5. 782109 (X), 6…. Status: Ongoing.
On the record
- Recalling firm
- Philips North America Llc
- Location
- Cambridge, MA
- Classification
- Class II
- Status
- Ongoing
- Recall number
- Z-3237-2026
- Product type
- Devices
- Recall initiated
- 2026-08-21
- Reported by FDA
- 2026-09-30
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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