Johnson & Johnson Surgical Vision, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1755-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.
Product Description:

Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge REF OPOHF21L The irrigation sleeve is a device intended to direct irrigation solution across the shaft of a phacoemulsification tip, allowing the solution to enter the eye during ocular surgery.

Product Classification:

Class II

Date Initiated: March 14, 2024
Date Posted: May 8, 2024
Recall Number: Z-1755-2024
Event ID: 94231
Reason for Recall:

Due to a manufacturing variation of the irrigation sleeves which could result in a missing port hole, this non-conformity could lead to insufficient flow to cool the ultrasonic phaco tip, potentially leading to an unstable anterior chamber which could cause possible harms.

Status: Ongoing
Product Quantity: 3,428 units
Code Information:

Part Number: OPOHF21L UDI-DI/GTIN code: 05050474573376 Lot Numbers: 60477723 60479361 60505085 60508179 60508923

Distribution Pattern:

U.S. Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, LA, MA, MD, ME, MN, MO, NC, NJ, NY, OR, PA, SC, TX, VA, WA, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated