Medline recalls lithotomy convenience kits with potential seal breaches in sterile pouches. Affected kits may risk contamination during surgery. Return or contact for replacement.
Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
Medline is recalling certain lithotomy surgical kits because some sterile pouches have openings in their seals. This could allow contamination during procedures, making the kits unsafe for use.
The sterile pouches in some kits have openings in their seals. This could allow contaminants to enter the surgical field during procedures, potentially causing infections or other complications.
Medical professionals using Medline lithotomy kits with the specific model number DYNJ50099C are affected. Surgeons and surgical teams at hospitals or clinics using these kits are most at risk.
Check for the model number DYNJ50099C on the kit. The kits were sold with GTIN 4019532701228 and lot number 22DBL482.
Inspect the sterile pouches for openings in the seal. If found, stop using the kit immediately.
Reach out to Medline for a replacement kit or instructions on how to return the affected product.
Medline received complaints about openings in the sterile pouch seals of some kits, which could lead to contamination during surgical procedures.
Check for the model number DYNJ50099C on the kit. Affected kits have GTIN 4019532701228 and lot number 22DBL482.
Inspect the pouch seals for openings. If you find openings, stop using the kit and contact Medline for a replacement or return instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0162-2023 — Medline Medline Hello, I own a Medline that is covered by recall Z-0162-2023 from Medline. 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.
