ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Reported: May 4, 2022 Initiated: March 16, 2022 #Z-1007-2022
Product Description
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.
Details
- Recalling Firm
- Carl Zeiss Meditec AG
- Units Affected
- 1225 devices
- 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
- Location
- Oberkochen
Frequently Asked Questions
What product was recalled? ▼
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.. Recalled by Carl Zeiss Meditec AG. Units affected: 1225 devices.
Why was this product recalled? ▼
High friction of the slider can cause the device to stick, or not move as intended.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 4, 2022. Severity: Moderate. Recall number: Z-1007-2022.
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