Ottobock recalls 21Y14=S PushValve upper parts (sold May 2017-Jan 2018) due to valve inserts that may be too small, risking improper prosthetic fitting for lower limb amputees.
Some of the installed valve-inserts have a diameter smaller than the specification.
Ottobock is recalling certain PushValve upper parts for prosthetic fittings because some valve inserts are too small. This could cause improper prosthetic function, potentially leading to discomfort or injury for lower limb amputees using the device.
The valve inserts may be smaller than specified, which could cause improper air evacuation from the prosthetic socket. This might lead to discomfort or improper function during use, but does not typically cause serious injury in normal use.
Lower limb amputees using Ottobock prosthetic fittings with the recalled PushValve upper parts. Those who purchased the product between May 1, 2017 and January 19, 2018 are most at risk.
Check for the product code 21Y14=S PushValve upper part. The product was sold between May 1, 2017 and January 19, 2018.
Look for the product code 21Y14=S PushValve upper part on the item.
Some valve inserts in the 21Y14=S PushValve upper parts are smaller than specified, which could cause improper air evacuation from the prosthetic socket.
The recall does not specify a remedy, so check with Ottobock Orthopedic Industrie for further instructions.
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-0827-2019 — Ottobock Ottobock Hello, I own a Ottobock that is covered by recall Z-0827-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.