V6-2 Transducer Probe Labeling Recall for Useful Life Clarification
Philips is recalling 171,322 V6-2 Transducer Probes nationwide to provide labeling clarification defining their useful life. No injuries have been reported.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: FDA Class III recall involving a labeling and documentation issue with no reported injuries, illnesses, or safety hazards. This is a clarification matter regarding product useful life specifications.
Plain-English summary
Philips Ultrasound, Inc. is recalling V6-2 Transducer Probes. The purpose of the recall is to provide clarification and labeling to define the useful life of ultrasound transducers in the field.
The recall affects 171,322 units that have been distributed nationwide in the United States. Affected devices include multiple model numbers and serial numbers as specified by the manufacturer.
The recalled product
- Product
- V6-2 Transducer Probe
- Manufacturer
- Philips Ultrasound, Inc
- Hazard
- labeling-clarification
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.
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