---
title: "REF: 126590, MEDLINE, STERILE ULTRASOUND GEL, 0.70 FL oz. (20 mL), QTY: 50, S... — FDA record Z-0777-2024 | Is It on Recall"
description: "Sterility of Ultrasound gel can not be guaranteed."
url: https://isitonrecall.com/recall/fda-device-z-0777-2024-ref-126590-medline-sterile-ultrasound-gel-0-70-fl-oz-20-ml-qty-50-steriler-ce-2292/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# REF: 126590, MEDLINE, STERILE ULTRASOUND GEL, 0.70 FL oz. (20 mL), QTY: 50, STERILER, CE 2292 — FDA record Z-0777-2024

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 Jun 9, 2023. 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**: REF: 126590, MEDLINE, STERILE ULTRASOUND GEL, 0.70 FL oz. (20 mL), QTY: 50, STERILER, CE 2292
- **Reason**: Sterility of Ultrasound gel can not be guaranteed.
- **Classification**: Class II
- **Recalling firm**: Turkuaz Saglik Hizmetleri Medikal Temizlik Kim. Ur. San. ve Tic. A.S.
- **Quantity**: 4,923,471
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0777-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0777-2024%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 | Lot Nos. SJ10091019 SJ22111019 SJ01041120 SJ25081020 SJ25061020 SJ20111020 SJ11021021 SJ24061021 SJ03061021 SJ14071021 SJ20091021 SJ09091021 SJ06022023 SJ10091019 |

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

## Distribution

US distribution to: Illinois and OUS (foreign) distribution to: Hong Kong

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

- [Illinois](https://isitonrecall.com/state/illinois/)

## Dates in the source

- **Report date**: Jan 31, 2024
- **Recall initiation date**: Jun 9, 2023
- **Center classification date**: Jan 20, 2024

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-0777-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Turkuaz Saglik Hizmetleri Medikal Temizlik Kim. Ur. San. ve Tic. A.S. records](https://isitonrecall.com/brand/turkuaz-saglik-hizmetleri-medikal-temizlik-kim-ur-san-ve-tic-a-s/)