Ottobock 21Y15 MagValve Recall: Small Valve Diameter Risk

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Recalling firmOttobock Orthopedic IndustrieMax-Nader Str 15 D-37ns, N/A · Duderstadt, N/A N/A

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Ottobock is recalling 21Y15 MagValves used in lower limb prosthetics because some valves have a diameter smaller than required. This could cause improper fitting or malfunction in prosthetic sockets.

Why it’s dangerous

The valve diameter is smaller than specified, which may cause improper fitting or malfunction in prosthetic sockets. This could lead to discomfort or improper function but does not typically cause serious injury.

Who’s affected

Users of lower limb prosthetics with the 21Y15 MagValve model sold between May 2017 and January 2018. Amputees using these valves are most at risk.

How to tell if you have this one

Check for the product code 21Y15 MagValve on the valve itself. The product was sold between May 1, 2017 and January 19, 2018.

Brand
Ottobock
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Valve Size
Verify the valve diameter matches the specified size on the product label.

✎ GovInfoNow

Questions people ask

Do I need to stop using this valve immediately?

The recall does not require immediate stop use; check the valve size before continuing use.

What should I do if the valve is too small?

The official notice does not specify a replacement or repair process.

When was this product sold?

The product was sold between May 1, 2017 and January 19, 2018.

Take action

Contact Ottobock

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

✉️ Open in email

Subject: Recall Z-0828-2019 — Ottobock Ottobock

Hello,

I own a Ottobock that is covered by recall Z-0828-2019 from Ottobock.

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-0828-2019 (January 10, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0828-2019 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.

Ottobock Orthopedic Industrie recalls 21Y15 MagValve Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower

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