Rayner Intraocular Lenses Limited: Medical Device Recall in 2020 - (Recall #: Z-1753-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Usage: The single use injectors (Model STWOl and Model RSPOl) are intended to be used to compress and insert into the capsular bag only those intraocular lenses that allow the use of these injectors in their approved labelling.

Product Classification:

Class II

Date Initiated: March 17, 2020

Date Posted: April 29, 2020

Recall Number: Z-1753-2020

Event ID: 85270

Reason for Recall:

RaySert PLUS RSP01 LOT K030 labeled with an expiry of 2024-01 contained an inner tray that was labeled with an expiry of 2015. In addition to having an expiry of 2015 the LOT number on the inner tray is identified as V001.

Status: Ongoing

Product Quantity: 2425 Units.

Code Information:

LOT K030.

Distribution Pattern:

US nationwide distribution in the states of OH, FL, GA, MD, SC, NJ, PR, IN, ID and MN.

Voluntary or Mandated:

Voluntary: Firm initiated