Ortho Solutions recalls System 26 Forefoot and Midfoot Implants and Instruments trays due to corrosion residue inside the cannulated devices. Affected units include specific part numbers and lot numbers sold in the US market.
Following the identification of corrosion residue found inside the cannulated devices in Forefoot and Midfoot trays Orhto Solutions Group has taken the decision to recall ALL x106 System 26 Forefoot and Midfoot Implants and Instruments tray from the US market.
Ortho Solutions is recalling all System 26 Forefoot and Midfoot Implants and Instruments trays sold in the US because corrosion residue was found inside the cannulated devices. This could pose a risk to users during medical procedures.
Corrosion residue found inside the cannulated devices could lead to contamination or damage during medical procedures. This residue may affect the safety and effectiveness of the implants and instruments.
Ortho Solutions System 26 Forefoot and Midfoot Implants and Instruments trays sold in the US market are affected. Patients and medical professionals using these devices are at risk due to potential corrosion residue.
Check for part numbers OS900035-NS through OS900059-NS or lot numbers listed in the recall notice. The affected products were sold in the US market starting from the specified dates.
Identify your System 26 Forefoot and Midfoot Implants and Instruments trays using the part numbers or lot numbers listed in the recall notice.
Part numbers OS900035-NS through OS900059-NS are affected.
Lot numbers 1088402 through 1091622 are affected.
The recall notice does not specify a remedy.
We’ve drafted a message you can send Ortho Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-0967-2018 — Ortho Solutions Ortho Solutions Hello, I own a Ortho Solutions that is covered by recall Z-0967-2018 from Ortho Solutions. 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.
