The affected lots are being recalled because the epiphysis may not assemble to the stem, which may cause a surgical delay.
The affected lots are being recalled because the epiphysis may not assemble to the stem, which may cause a surgical delay.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send DePuy Orthopaedics, Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-0833-2018 — DePuy Orthopaedics, Inc. DePuy Orthopaedics, Inc. recalls DELTA XTEND" Reverse Shoulder System Modu Hello, I own a DePuy Orthopaedics, Inc. recalls DELTA XTEND" Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants are intended for use in total that is covered by recall Z-0833-2018 from DePuy Orthopaedics, Inc.. 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.
