DeP: Hip Prosthesis Recall - Incorrect Part Number Risk

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Contact the company & request your remedy

Recalling firmDePuy Orthopaedics, Inc.700 Orthopaedic Dr, N/A · Warsaw, IN 46582-3994

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

DePuy is recalling 50 hip implants that have the wrong part number and size marked on them. This could lead to improper fitting if used, which might cause complications during surgery or after implantation.

Why it’s dangerous

The recalled implants have incorrect part numbers and sizes etched on them. This could lead to improper fitting during surgery or after implantation, potentially causing complications.

Who’s affected

Patients who received the specific hip implant model with Lot D20111130 and part number 1365-21-000 are affected. Those with this exact model and lot number are at risk of improper fit.

How to tell if you have this one

Check for the part number 1365-21-000 and lot number D20111130 on the implant. The product is a hip joint metal/polymer semi-constrained cemented prosthesis.

Brand
DePuy
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the part number and lot number on the implant to confirm if it matches the recalled model.

✎ GovInfoNow

Questions people ask

How many units are being recalled?

50 units with the incorrect part number and size etched on the product.

What is the specific part number for the recalled implants?

Part number 1365-21-000 with lot number D20111130.

Do I need to stop using the implant?

The recall does not require stopping use; it's about verifying the correct part number and lot number.

Take action

Contact DePuy

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

✉️ Open in email

Subject: Recall Z-1845-2021 — DePuy DePuy

Hello,

I own a DePuy that is covered by recall Z-1845-2021 from DePuy.

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-1845-2021 (May 7, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1845-2021 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.

DePuy Orthopaedics, Inc. recalls DePuy Synthes Articul/eze Femoral Head: Hip joint metal/polymer semi-constrained cemented prosthesis. Part Number:

Lower-risk recall