Johnson & Johnson Surgical Vision, Inc. 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. Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Johnson & Johnson Surgical Vision, Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Part Number: OPOHF21L UDI-DI/GTIN code: 05050474573376 Lot Numbers: 60477723 60479361 60505085 60508179 60508923
Johnson & Johnson Surgical Vision, Inc. is recalling Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge RE due to Due to a manufacturing variation of the irrigation sleeves which could result in a missing port hole, this non-conformity could lead to insufficient f. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
On 03/11/2024, the firm sent an "URGENT: MEDICAL DEVICE RECALL" Letter via FedEx 2-Day Mail Delivery to customers informing them that due to a manufacturing issue with the Irrigation Sleeves which could result in a missing or incompletely cut port hole. A missing hole or incompletely cut port hole is visible on inspection with the naked eye and can also be functionally detected prior to surgery, if and when, the user engages the irrigation function in accordance with the Directions for Use. A completely missing port hole will result in a priming error prior to surgery. This could lead to intraoperative delay in surgery or even rescheduling of surgery in case there are no back up phacoemulsification sleeves available in the surgical site. Customers are instructed to: 1. Identify if any of their inventory contains Irrigation Sleeves with any of the five lot numbers. 2. Remove and Do Not Use affected Irrigation Sleeves from your inventory, regardless of whether the Irrigation Sleeves visually appear acceptable. No other Irrigation Sleeves are affected by this recall and can continue to be used. If you have product to be returned: " Complete the Customer Reply Form, noting the lot numbers of the Irrigation Sleeves. " Contact Customer Support at 1-877-266-4543 Option 2 to obtain an RGA number and arrange the product return. " Email Customer Reply Form to RegCompliOne@its.jnj.com within 3 business days of receipt of this letter. " Return the affected product as soon as possible. A credit will be issued upon receipt of the customer reply form and product. If you do not have product to be returned: " Complete and return the Customer Reply Form and email to RegCompliOne@its.jnj.com within 3 business days of receipt of this letter. For questions or concerns, contact 1-877-266-4543 Option 2.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026