The Recall Desk
Severity pendingFDA (Devices)·Z-2403-2025·Announced 2025-09-03

V6-2 Transducer Probe

Pending LLM rewrite. Source: FDA_DEVICE Z-2403-2025.

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
V6-2 Transducer Probe
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. 989605415042
  • 989605437982
  • 989605438461
  • 989605357563
  • 989605357561
  • 989605387201
  • 989605415041
  • 989605449011
  • 989605395631
  • 989605454101
  • UDI: (01)00884838061460(21)B1VJQF
  • (01)00884838061460(21)B2RL4B
  • (01)00884838061651(21)B20WVG
  • (01)00884838061651(21)B28DGB
  • (01)00884838061651(21)B304XN
  • (01)00884838061651(21)B35CH3
  • (01)00884838061651(21)B20WW0
  • (01)00884838061651(21)B1YQQ6
  • (01)00884838061651(21)B1XLYC
  • (01)00884838061651(21)B1YQZR

Distribution

Distributed nationwide across the United States.

Related recalls

Same category