DePuy Mitek recalls Latarjet Experience Instability Shoulder Sets due to reports of loosening or unscrewing from the handle. Affected models include 16D01, 16D02, 16K01, 17A01, 17B01, 17B02.
Reports of product loosening or coming unscrewed from the handle.
DePuy Mitek is recalling Latarjet Experience Instability Shoulder Sets after reports of the product loosening or coming unscrewed from the handle. This could lead to improper bone fixation during surgery, potentially causing complications.
The product can loosen or come unscrewed from the handle during use, which may result in improper bone fixation. This could cause surgical complications if the device fails to stay securely attached during procedures.
Orthopedic surgeons who use the Latarjet Experience Instability Shoulder Set for bone fixation during reconstructive surgeries are most at risk. The recall affects specific model numbers sold in the U.S.
Check for model numbers 16D01, 16D02, 16K01, 17A01, 17B01, or 17B02 on the product. The Latarjet Experience Instability Shoulder Set is used by orthopedic surgeons for bone fixation in reconstructive surgeries.
Look for model numbers 16D01, 16D02, 16K01, 17A01, 17B01, or 17B02 on the product.
The recall is due to reports of the product loosening or coming unscrewed from the handle, which could lead to improper bone fixation during surgery.
Affected models include 16D01, 16D02, 16K01, 17A01, 17B01, and 17B02.
The recall does not require immediate discontinuation; however, users should check model numbers and follow the provided steps to ensure safety.
We’ve drafted a message you can send DePuy Mitek to request your refund or repair — edit it as you like.
Subject: Recall Z-1749-2018 — DePuy Mitek DePuy Mitek Hello, I own a DePuy Mitek that is covered by recall Z-1749-2018 from DePuy Mitek. 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.
