Zimmer Biomet recalls T7 Driver Solid AO (Part 110018541) used in foot and hand surgeries due to potential fracture, bending, or shearing of the driver component.
There is a potential of fracture, bending or shearing of the driver.
Zimmer Biomet is recalling T7 Driver Solid AO parts used in foot and hand surgeries because there's a risk of the driver component fracturing, bending, or shearing during use. This could lead to complications in surgical procedures if not addressed.
The driver component can fracture, bend, or shear during surgical procedures, which may cause complications in bone fixation or joint fusion. This risk occurs when the device is used in the foot or hand to correct conditions like bunions or toe deformities.
Surgical patients and medical professionals who have received the T7 Driver Solid AO (Part Number 110018541) for foot or hand procedures are affected. Those using the device in surgeries are most at risk.
Check if your device has the part number 110018541 and lot numbers listed: 13421A, 13811A, 14042B, 14048B, 14140A, 14194B, 14343A, 14392A, 14393A, 14394A, 14518A, 14601A, 14827B, 14895C, 15015B, 15167B, 15257A, 15392A.
Look for the lot numbers listed: 13421A, 13811A, 14042B, 14048B, 14140A, 14194B, 14343A, 14392A, 14393A, 14394A, 14518A, 14601A, 14827B, 14895C, 15015B, 15167B, 15257A, 15392A.
The part number is 110018541.
This device is used for fixation of bone fractures, fusion of joints, or bone reconstruction in the foot or hand, including procedures for bunions, toe deformities, and joint issues.
Check the lot number on your device. If it matches the listed numbers, contact Zimmer Biomet for further instructions.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1303-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1303-2019 from Zimmer Biomet. 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.
