Carl Zeiss Meditec AG: Medical Device Recall in 2022 - (Recall #: Z-1007-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 16, 2022

Date Posted: May 4, 2022

Recall Number: Z-1007-2022

Event ID: 89928

Reason for Recall:

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

Status: Ongoing

Product Quantity: 1225 devices

Code Information:

Model: 303071-9090-000 Catalog Number: FG-50608 UDI: (01)04049539104496(11)201102(17)231031(10)FG21082410 Lot Number: FG21082410

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated