Rayner Intraocular Lenses Limited: Medical Device Recall in 2018 - (Recall #: Z-3282-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

C-flex 570C +19.0D Intraocular Lens Product Usage: C-flex IOLs are designed to be surgically implanted into the capsular bag of the human eye as a replacement for the crystalline lens following phacoemulsification

Product Classification:

Class II

Date Initiated: August 9, 2018

Date Posted: October 10, 2018

Recall Number: Z-3282-2018

Event ID: 80943

Reason for Recall:

Firm become aware of reports of post-operative refractive errors following implantation of lenses.

Status: Terminated

Product Quantity: 49

Code Information:

Batch 017100825 Lens #'s: 01710082501, 01710082502, 01710082503, 01710082504, 01710082505, 01710082506, 01710082507, 01710082508, 01710082509, 01710082510, 01710082511, 01710082512, 01710082513, 01710082514, 01710082515, 01710082516, 01710082517, 01710082518, 01710082519, 01710082520, 01710082521, 01710082522, 01710082523, 01710082524, 01710082525, 01710082526, 01710082527, 01710082528, 01710082529, 01710082530, 01710082531, 01710082532, 01710082533, 01710082534, 01710082535, 01710082536, 01710082537, 01710082538, 01710082539, 01710082540, 01710082541, 01710082542, 01710082543, 01710082544, 01710082545, 01710082546, 01710082547, 01710082548, and 01710082549.

Distribution Pattern:

US in the states of MO

Voluntary or Mandated:

Voluntary: Firm initiated