Ottobock PushValve 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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Ottobock is recalling certain PushValves used in lower limb prosthetics because some valve inserts have a diameter smaller than required. This could lead to improper air evacuation from the prosthetic socket, potentially causing discomfort or malfunction.

Why it’s dangerous

The valve inserts have a smaller diameter than specified, which may not evacuate air properly from the prosthetic socket. This could cause improper fit or function of the prosthetic device, but does not pose an immediate risk of injury.

Who’s affected

Prosthetic users with the specific model 21Y14 PushValves purchased between May 1, 2017 and January 19, 2018 are affected. Those with lower limb amputations using these valves are most at risk.

How to tell if you have this one

Check for the product name '21Y14 PushValve' on the packaging or label. 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 Insert Size
Inspect the valve insert for a diameter smaller than specified. If unsure, contact Ottobock for verification.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

Some valve inserts have a diameter smaller than the specification, which may not evacuate air properly from the prosthetic socket.

What should I do if I have this product?

Check if your valve insert is smaller than specified. If unsure, contact Ottobock for verification.

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-0826-2019 — Ottobock Ottobock

Hello,

I own a Ottobock that is covered by recall Z-0826-2019 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-0826-2019 (January 10, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0826-2019 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 21Y14 PushValve Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower

Lower-risk recall