Philips Mini Multi TEE Ultrasound Transducer
Pending LLM rewrite. Source: FDA_DEVICE Z-1622-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
The recalled product
- Product
- Philips Mini Multi TEE Ultrasound Transducer
- Manufacturer
- Philips Ultrasound, Inc
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Model No. 989605439241
- 989605439242
- 21381A
- UDI: (01)00884838067547(21)B093BQ
- (01)00884838067547(21)B0988T
- (01)00884838067547(21)02P6MY
- (01)00884838067547(21)039M2Q
- (01)00884838067547(21)0319CQ
- (01)00884838067547(21)B01639
- Serial No. 02GXR0
- B093BQ
- B0988T
- 02P6MY
- 039M2Q
- 0341YT
- 0319CQ
- 028NZW
- 02H0L8
- B01639
- 039M2M.
Distribution
Distributed nationwide across the United States.
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