# FDA recall Z-1007-2022

> **Carl Zeiss Meditec AG** · Class II · device recall initiated 2022-03-16.

## Product

ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.

## Reason for recall

High friction of the slider can cause the device to stick, or not move as intended.

## 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

## Key facts

- **Recall number:** Z-1007-2022
- **Recalling firm:** Carl Zeiss Meditec AG
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-03-16
- **Report date:** 2022-05-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oberkochen, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1007-2022

## Citation

> AI Analytics. FDA recall Z-1007-2022. Retrieved 2026-06-01 from https://api.ai-analytics.org/recall/Z-1007-2022. Source: US FDA. Licensed CC0.

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