Ottobock recalls 21Y15 MagValves for lower limb prosthetics sold 2017-2018 due to valve diameter smaller than spec. Affected users should check product details.
Some of the installed valve-inserts have a diameter smaller than the specification.
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.
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.
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.
Check for the product code 21Y15 MagValve on the valve itself. The product was sold between May 1, 2017 and January 19, 2018.
Verify the valve diameter matches the specified size on the product label.
The recall does not require immediate stop use; check the valve size before continuing use.
The official notice does not specify a replacement or repair process.
The product was sold between May 1, 2017 and January 19, 2018.
We’ve drafted a message you can send Ottobock to request your refund or repair — edit it as you like.
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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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.
