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FDA · Medical devices ·

Convenience kits CATARACT PACK DYNJ59881A recall

Medline Industries, LP recalled Convenience kits CATARACT PACK DYNJ59881A on September 23, 2026 because of kits may exhibit open seals in sterile pouch packaging. It was sold nationwide.

Why it was recalled

Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.

What's recalled

Convenience kits CATARACT PACK DYNJ59881A

Quantity: 336

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Medline Industries, LP, Northfield, IL
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.
Status
Ongoing
Recall number
Z-3210-2026
Source
U.S. Food and Drug Administration

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