---
title: "ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during catar... — FDA record Z-1007-2022 | Is It on Recall"
description: "High friction of the slider can cause the device to stick, or not move as intended."
url: https://isitonrecall.com/recall/fda-device-z-1007-2022-zeiss-miloop-lens-fragmentation-device-ref-303071-9090-000-used-during-cataract-surgery/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery. — FDA record Z-1007-2022

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 Mar 16, 2022. 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**: ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
- **Reason**: High friction of the slider can cause the device to stick, or not move as intended.
- **Classification**: Class II
- **Recalling firm**: Carl Zeiss Meditec AG
- **Quantity**: 1225 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1007-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1007-2022%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: 303071-9090-000 Catalog Number: FG-50608 UDI: (01)04049539104496(11)201102(17)231031(10)FG21082410 Lot Number: FG21082410 |

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

## Distribution

U.S.: AL, AR, AZ, CA, CT, FL, GA, IA, IL, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NJ, NY, OH, OR, PA, Puerto Rico, SC, TN, TX. UT, VA, WA, and WV O.U.S.: Not provided

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

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- [West Virginia](https://isitonrecall.com/state/west-virginia/)

## Dates in the source

- **Report date**: May 4, 2022
- **Recall initiation date**: Mar 16, 2022
- **Center classification date**: Apr 26, 2022

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-1007-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Carl Zeiss Meditec AG records](https://isitonrecall.com/brand/carl-zeiss-meditec-ag/)