Medline Cataract Tray Recall: Breach in Sterile Kit Pouch Seal

Take action

Contact the company & request your remedy

Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr, N/A · Northfield, IL 60093-2753

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Medline is recalling cataract surgical trays that have reported openings in the sterile pouch seals. This could allow contamination during surgery, making the kits unsafe for use.

Why it’s dangerous

The sterile pouch seals on some cataract surgical kits have openings. This could allow contaminants to enter the surgical field during procedures, risking infection.

Who’s affected

Surgical teams using the recalled cataract trays for eye procedures. Patients undergoing surgery with these kits face potential infection risks.

How to tell if you have this one

Check for the model reference LYN023FACTB on the tray. The kits were sold with GTIN 10889942339730 and lot number 22DBM506.

Brand
Medline
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Kit Seal
Inspect the sterile pouch for openings in the seal before use.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

Medline received complaints about openings in the sterile pouch seals of some cataract surgical kits.

How can I tell if I have the recalled product?

Look for the model reference LYN02:3FACTB on the tray, with GTIN 10889942339730 and lot number 22DBM506.

What should I do if I have the recalled product?

The recall record does not specify a remedy, so contact Medline directly for guidance.

Take action

Contact Medline

We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0160-2023 — Medline Medline

Hello,

I own a Medline that is covered by recall Z-0160-2023 from Medline.

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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Where this comes from

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.

Official source: FDA Recall #Z-0160-2023 (September 30, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0160-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

MEDLINE INDUSTRIES, LP - Northfield recalls BAUSCH + LOMB CATARACT TRAY, REF LYN023FACTB. Convenience kit used in surgical procedures.

Use caution until it’s fixed