Medline recalls Rhino Plasty Pack convenience kits (model DYNJ27333F) due to potential weak seals on breather pouches that could lead to contamination during procedures.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling Rhino Plasty Pack convenience kits (model DYNJ2:7333F) because the breather pouches might have weak seals. This could allow contaminants to enter the sterile kit during medical procedures, posing a risk to patient safety.
The breather pouches used to package the sterile kits may have open or weak seals. This could allow contaminants to enter the kit during medical procedures, potentially leading to infections or other complications.
Healthcare professionals using Medline Rhino Plasty Pack kits for procedures like rhinoplasty. Patients receiving these kits are at risk if the weak seals cause contamination.
Check for the model number DYNJ27333F on the kit. The lot number 24KBH228 and UDI-DI numbers 10888277055292 (each) and 40888277055293 (case) are also associated with this recall.
Verify the model number on the kit is DYNJ27333F.
The breather pouches used to package the sterile kits may have open or weak seals, which could allow contaminants to enter the kit during medical procedures.
The recall record does not specify a remedy, so no action is required beyond checking the model number.
The recall indicates a potential for contamination, but the record does not mention a risk of serious injury or death.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1596-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1596-2025 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.
