PlainRecalls
FDA Devices Moderate Class II Terminated

TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag.

Reported: March 10, 2021 Initiated: January 27, 2021 #Z-1163-2021

Product Description

TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag.

Reason for Recall

Due to the release of nonconforming Intraocular Lenses (IOLs).

Details

Units Affected
27 lenses
Distribution
U.S. Nationwide distribution in the states of AL, AZ, CA, FL, GA, IL, LA, MI, MN, NC, NY, OH, PA, SC, TN, TX, UT and WA.
Location
Santa Ana, CA

Frequently Asked Questions

What product was recalled?
TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag.. Recalled by Johnson & Johnson Surgical Vision Inc. Units affected: 27 lenses.
Why was this product recalled?
Due to the release of nonconforming Intraocular Lenses (IOLs).
Which agency issued this recall?
This recall was issued by the FDA Devices on March 10, 2021. Severity: Moderate. Recall number: Z-1163-2021.