Flower Orthoped: Recalls Calcaneus Plate (CPF 202) made with wrong titanium alloy. Risk of improper healing due to material error. Contact for remedy.
The contract manufacturer of the calcaneus plate inadvertently used the incorrect material to manufacture the plates (a titanium alloy rather than pure titanium).
Flower Orthopedics is recalling a specific calcaneus plate model because it was made with the wrong titanium alloy. This could lead to improper bone healing or complications if used in surgery.
The plate was manufactured with a titanium alloy instead of pure titanium. This material difference could cause improper bone healing or complications during surgery.
Patients who received this specific calcaneus plate for rearfoot fracture repair are affected. Surgeons and medical staff who used this model during procedures may also be at risk.
Check for the catalog number CPF 202 on the plate. The product was sold with lot number 1909660035 and UDI 00840118115681.
Look for the catalog number CPF 202, lot number 1909660035, and UDI 00840118115681 on the plate.
The recall states the plate was made with the wrong material, which could lead to improper healing. However, the remedy is not specified in the record.
Check for the catalog number CPF 202, lot number 1909660035, and UDI 00840118115681 on the plate.
The recall record does not specify a remedy, so contact Flower Orthopedics for guidance.
We’ve drafted a message you can send Flower Orthopedics to request your refund or repair — edit it as you like.
Subject: Recall Z-2786-2020 — Flower Orthopedics Flower Orthopedics Hello, I own a Flower Orthopedics that is covered by recall Z-2786-2020 from Flower Orthopedics. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
