Centurion Medical recalls IV Start Kits with specific lot numbers due to potential risk of improper IV placement during medical procedures.
Convenience Kit containing components to assist practitioner with IV placement and securement.
Centurion Medical is recalling certain IV Start Kits that may not secure properly during IV placement, which could lead to improper medical treatment. This recall affects healthcare professionals and patients receiving IV therapy.
The IV Start Kits may not secure properly during IV placement, potentially leading to improper medical treatment. This could cause complications if the IV line becomes dislodged or improperly connected.
Healthcare professionals and patients receiving IV therapy using the recalled kits are most at risk. The recall targets specific lot numbers produced between 2015 and 2017.
Check the lot numbers on the kit: 2015110290, 2016011190, 2016030790, 2016050290, 2016061390, 2016081590, 2016101090, 2017010290, 2017021390, 2017032090, 2017050890, 2017071790, 2015110990, 2016020890, 2016062090, 2016071190, 2016072590, 2016080890, 2016082990, 2016090590, 2016091990.
Look for the specific lot numbers listed in the recall notice on the IV Start Kit packaging.
Centurion Medical is recalling certain IV Start Kits that may not secure properly during IV placement, potentially leading to improper medical treatment.
The affected lot numbers are: 2015110290, 2016011190, 2016030790, 2016050290, 2016061390, 2016081590, 2016101090, 2017010290, 2017021390, 2017032090, 2017050890, 2017071790, 2015110990, 2016020890, 2016062090, 2016071190, 2016072590, 2016080890, 2016082990, 2016090590, 2016091990.
The recall does not require immediate discontinuation; check the lot numbers to determine if your kit is affected.
We’ve drafted a message you can send Centurion Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1093-2018 — Centurion Medical Centurion Medical Hello, I own a Centurion Medical that is covered by recall Z-1093-2018 from Centurion Medical. 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.
