Ethicon Curved Staplers May Not Form Staples Properly - Recall

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Recalling firmEthicon Endo-Surgery Inc4545 Creek Rd · Blue Ash, OH 45242-2803

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Ethicon is recalling curved intraluminal staplers (model CDH25A, 25mm diameter) because they might not form staples properly. This could lead to incomplete tissue joining during surgery, potentially causing complications.

Why it’s dangerous

The staplers may not fully form staples because the firing stroke is too short. This could result in incomplete tissue attachment during surgical procedures, potentially causing leaks or complications.

Who’s affected

Surgical professionals using these staplers for procedures involving tissue joining. The risk is primarily for medical staff handling the instruments during surgery.

How to tell if you have this one

Check for the model CDH25A with a 25mm diameter. These staplers were sold between December 2022 and March 2024.

Brand
Ethicon
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify if your stapler is model CDH25A with 25mm diameter.

✎ GovInfoNow

Questions people ask

Why is this stapler being recalled?

The staplers may have an insufficient firing stroke to break the washer and completely form staples.

What should I do if I have this stapler?

The recall does not specify a remedy, so check with Ethicon Endo-Surgery for guidance.

When were these staplers sold?

These staplers were sold between December 2022 and March 2024.

Take action

Contact Ethicon

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

✉️ Open in email

Subject: Recall Z-1268-2019 — Ethicon Ethicon

Hello,

I own a Ethicon that is covered by recall Z-1268-2019 from Ethicon.

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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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-1268-2019 (April 11, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1268-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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.

Ethicon Endo-Surgery Inc recalls Curved Intraluminal Staplers, 25 mm diameter, Model CDH25A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are

Lower-risk recall