Zimmer recalls M/L Taper Hip Prosthesis with Kinectiv Technology (size 5) made before Oct 2015 due to potential black residue in polyethylene bags. This residue may delay surgery or cause wear from debris.
M/L Taper Hip Prosthesis and M/L Taper Hip Prosthesis with Kinectiv Technology manufactured prior to October 2015 are being recalled due to the potential for black residue to be observed within the polyethylene bag containing the implant. The black residue is a combination of the titanium plasma spray used to create the porous surface of the implant and polyethylene bag containing the implant. The recalling firm states the residue is biocompatible. Risks include delay of surgery while locating a replacement device, and surgical intervention due to wear caused by debris.
Zimmer is recalling hip implants with Kinectiv technology made before October 2015 because black residue in the packaging could delay surgery or cause implant wear. This affects patients who received these specific implants.
The black residue comes from titanium plasma spray and the polyethylene bag. While the residue is biocompatible, it can cause delays in surgery or lead to implant wear due to debris during the procedure.
Patients who received the recalled Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology (size 5) made before October 2015 are most at risk. The recall targets individuals who have this specific implant.
Check for the model number 00-7713-005-00 on the implant packaging. The recall applies to implants manufactured before October 2015.
Look for the model number 00-7713-005-00 on the implant packaging to confirm if it's recalled.
The recall states the black residue is biocompatible, but it may delay surgery or cause implant wear, so patients should follow the recall instructions.
Check the implant packaging for the model number 00-7713-005-00. If it matches, contact Zimmer for further instructions.
The black residue is a combination of titanium plasma spray used to create the porous surface and the polyethylene bag material.
We’ve drafted a message you can send Zimmer to request your refund or repair — edit it as you like.
Subject: Recall Z-2363-2018 — Zimmer Zimmer Hello, I own a Zimmer that is covered by recall Z-2363-2018 from Zimmer. 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.
