---
title: "Philips X6-1 Transducer. — FDA record Z-2065-2025 | Is It on Recall"
description: "Ultrasound transducer devices were refurbished beyond their useful life."
url: https://isitonrecall.com/recall/fda-device-z-2065-2025-philips-x6-1-transducer/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Philips X6-1 Transducer. — FDA record Z-2065-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 28, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Philips X6-1 Transducer.
- **Reason**: Ultrasound transducer devices were refurbished beyond their useful life.
- **Classification**: Class II
- **Recalling firm**: Philips Ultrasound, Inc
- **Quantity**: 5,230 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2065-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2065-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model No. 989605409282, 989605438511, 989605357143, 989605357141; UDI: (01)00884838061446(21)B1HT1C, (01)00884838061446(21)B1HT47, (01)00884838061446(21)B1W368, (01)00884838061446(21)B1WBDL, (01)00884838061446(21)B1GTFL, (01)00884838061446(21)B11YW3, (01)00884838061446(21)B15QX1, (01)00884838061446(21)B14LVN, (01)00884838061446(21)B22R48, (01)00884838061446(21)B11XQP, (01)00884838061446(21)B1HTJ3, (01)00884838061446(21)B11Z3B, (01)00884838061446(21)B0WX2W, (01)00884838061446(21)B0WYZ1, (01)00884838061446(21)B131LH, (01)00884838061446(21)B1C1C3, (01)00884838061446(21)B1JBBF, (01)00884838061446(21)B101WK, (01)00884838061446(21)B14M20, (01)00884838061446(21)B1GVWH, (01)00884838061446(21)B1H6V3, (01)00884838061446(21)B101TF, (01)00884838061446(21)B1JCYV, (01)00884838061446(21)B2HQD0, (01)00884838061446(21)B27YP9, (01)00884838061446(21)B21DZ3, (01)00884838061446(21)B0Z7G7, (01)00884838061446(21)B0V082, (01)00884838061446(21)B22QVL, (01)00884838061446(21)B14MMW, (01)00884838061446(21)B24VGG, (01)00884838061446(21)B21CGY, (01)00884838061446(21)B1GTDB, (01)00884838061781(21)B157R5, (01)00884838061781(21)B1903C, (01)00884838061781(21)B187M7, (01)00884838061446(21)B21CH0, (01)00884838061781(21)B14MMX, (01)00884838061446(21)B2HQCW, (01)00884838061446(21)B18YDK, (01)00884838061781(21)B13R4G, (01)00884838061781(21)B11X02, (01)00884838061446(21)B18Z17, (01)00884838061446(21)B0V150, 010088483806144621B1WQHH; Serial No. B1HT1C, B1HT47, B1W368, B1WBDL, B1GTFL, B11YW3, B15QX1, B14LVN, B22R48, B11XQP, B1HTJ3, B11Z3B, B0WX2W, B0WYZ1, B131LH, B1C1C3, B1JBBF, B14P5W, B101WK, B14M20, B1GVWH, B1H6V3, B101TF, B1JCYV, B2HQD0, B27YP9, B21DZ3, B0Z7G7, B0V082, B22QVL, B132FF, B14MMW, B19075, B24VGG, B21CGY, B1GTDB, B157R5, B1903C, B1HTQB, B187M7, B0TZQM, B21CH0, B14MMX, B0Z7GF, B06HHH, B2HQCW, B18YDK, B13R4G, B131XX, B0WYDD, B0WYNP, B11X02, B18Z17, B1H9YQ, B1H9YR, B0V150, B1WQHH. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic: Nationwide Distribution; Foreign: Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Luxembourg, Malaysia, Mexico, Morocco, Netherlands, New Caledonia, New Zealand, Nicaragua, Oman, Philippines, Poland, Portugal, Romania, Russian Fed., Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Thailand, T¿rkiye, United Kingdom, United Arab Emirates, Venezuela, Vietnam.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jul 9, 2025
- **Recall initiation date**: May 28, 2025
- **Center classification date**: Jul 2, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2065-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Philips Ultrasound, Inc. records](https://isitonrecall.com/brand/philips-ultrasound-inc/)
