Johnson & Johnson Surgical Vision recalls Veritas Advanced Infusion Packs used in eye surgery due to broken irrigation luer fittings. Affected units have specific lot numbers. Consumers should contact the company for details.
As a result of returned product complaints for Veritas Phaco packs related to broken or cracked irrigation luer due to a manufacturing issue.
Johnson & Johnson Surgical Vision is recalling Veritas Advanced Infusion Packs used in eye surgery procedures because some units have a manufacturing defect that can cause irrigation luer fittings to break. This defect may lead to complications during surgery if the device is used without proper integrity.
The irrigation luer fitting in some Veritas Advanced Infusion Packs can break due to a manufacturing defect. This breakage could cause leaks or improper fluid flow during eye surgery, potentially leading to complications for the patient.
Medical professionals who use these infusion packs during eye surgery are most at risk. Patients undergoing ophthalmic procedures with the recalled product could face complications if the irrigation luer breaks during surgery.
Check the lot numbers on the product: 60316112, 60330206, 60330248, and other specific numbers listed in the recall notice. These packs are used in eye surgery procedures and are manufactured by Johnson & Johnson Surgical Vision.
Look for lot numbers on the Veritas Advanced Infusion Packs: 60316112, 60330206, 60330248, and other specific numbers listed in the recall notice.
The recall is due to a manufacturing defect that can cause irrigation luer fittings to break, which may lead to complications during eye surgery.
Check the lot numbers on the product to see if it's affected. If it is, contact Johnson & Johnson Surgical Vision for further instructions.
Yes, if the irrigation luer breaks during surgery, it could cause leaks or improper fluid flow, potentially leading to complications for the patient.
We’ve drafted a message you can send Johnson & Johnson Surgical Vision to request your refund or repair — edit it as you like.
Subject: Recall Z-0086-2023 — Johnson & Johnson Surgical Vision Johnson & Johnson Surgical Vision Hello, I own a Johnson & Johnson Surgical Vision that is covered by recall Z-0086-2023 from Johnson & Johnson Surgical Vision. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
