Zimmer Biomet recalls NexGen Complete Knee Solution Femoral Augment Block Distal only, 15mm, Size E with Screw (Item #00599003523) due to missing screw in package. Affected patients should contact manufacturer for details.
Screw is missing from the package
Zimmer Biomet is recalling a specific knee implant component because the package may be missing the screw. This could lead to improper installation and potential complications during surgery.
The screw is missing from the package, which could result in the implant not being properly secured during surgery. This might cause improper alignment or instability of the knee joint after the procedure.
Patients who received this specific knee implant component (NexGen Distal Femoral Augment Block) are affected. Surgeons and medical staff who used this component during procedures are at highest risk.
Check for the item number 00599003523 on the package. The product is a NexGen Complete Knee Solution Femoral Augment Block Distal only, 15mm, Size E with Screw. This was sold with lot number 62925336.
Verify that the screw is included in the package. If missing, contact Zimmer Biomet for further instructions.
The recall states the screw may be missing from the package, which could lead to improper installation during surgery. However, the hazard is not described as causing serious injury in normal use.
Look for the item number 00599003523 on the package. The product is a NexGen Complete Knee Solution Femoral Augment Block Distal only, 15mm, Size E with Screw, sold with lot number 62925336.
Contact Zimmer Biomet directly to check if the screw is missing and get instructions on next steps.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0630-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0630-2019 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.
