Howmedica Exeter V40 Hip Stem Recall: Potential Label Mixup

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Recalling firmHowmedica Osteonics Corp.325 Corporate Dr, N/A · Mahwah, NJ 07430-2006

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Howmedica is recalling Exeter V4:0 Cemented Hip (125mm) Stems due to a potential mix-up with 150mm stems. This could lead to incorrect implant size being used, which might cause complications during surgery.

Why it’s dangerous

The recall is for a potential mix-up between 125mm and 150mm stems. Using the wrong size stem could lead to improper fit during hip replacement surgery, potentially causing complications.

Who’s affected

Patients who received this specific stem during hip replacement surgery are affected. Surgeons and medical staff who used the recalled stem are at higher risk.

How to tell if you have this one

Check for the part number 0580-1-044 and lot number G7900236 on the stem. The product was sold with a GTIN: 04546540509048.

Brand
Howmedica
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the part number 0580-1-044 and lot number G7900236 on the stem.

✎ GovInfoNow

Questions people ask

Is this recall dangerous?

The recall is for a potential label mix-up between 125mm and 150mm stems, which could lead to incorrect implant size during surgery. However, the hazard is not described as causing serious injury in normal use.

How can I tell if I have the recalled stem?

Check for the part number 0580-1-044 and lot number G7900236 on the stem. The product was sold with a GTIN: 04546540509048.

What should I do if I have the recalled stem?

The recall does not specify a remedy, so no action is required beyond checking the label.

Take action

Contact Howmedica

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

✉️ Open in email

Subject: Recall Z-0651-2022 — Howmedica Howmedica

Hello,

I own a Howmedica that is covered by recall Z-0651-2022 from Howmedica.

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-0651-2022 (December 30, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0651-2022 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.

Howmedica Osteonics Corp. recalls Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044

Lower-risk recall