Zimmer Surgical recalls 3:1 Dermacarrier model 00219501300 skin graft carriers due to incorrect ridge ratio (1.5:1 instead of 3:1) which may cause minor tissue damage or unplanned grafts.
Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The problem may lead to minor tissue damage or additional unplanned graft if deemed necessary.
Zimmer Surgical is recalling skin graft carriers that have a manufacturing error in the ridge pattern ratio. This could lead to minor tissue damage or the need for additional grafts during medical procedures.
The carrier is labeled as 3:1 ratio but has a 1.5:1 ridge pattern. This mismatch may cause improper graft placement, leading to minor tissue damage or requiring additional grafts if the issue isn't corrected.
Patients using skin graft carriers for medical procedures. Those with the specific model number 00219501300 are most at risk.
Check for model number 00219501300 on the carrier. The product was sold with UDI-DI 00889024378780 and lots 65292843 (expires Oct 2026) or 65390419 (expires Jan 2027).
Look for model number 00219501300 on the carrier.
Due to a manufacturing issue where the ridge pattern ratio is 1.5:1 instead of the labeled 3:1 ratio, which may cause minor tissue damage or additional grafts.
Check the model number and lot information. If it matches the recalled items, contact Zimmer Surgical for further instructions.
The recall states the issue may lead to minor tissue damage or additional grafts, not serious injury. The danger level is low risk.
We’ve drafted a message you can send Zimmer Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1078-2024 — Zimmer Surgical Zimmer Surgical Hello, I own a Zimmer Surgical that is covered by recall Z-1078-2024 from Zimmer Surgical. 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.
