Medline recalls dental convenience kits with potential weak seals on breather pouches that could lead to contamination during procedures. Affected kits include specific models and lot numbers from 2024.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling dental convenience kits that may have weak seals on breather pouches. This could allow contaminants to enter the sterile kits during medical procedures, posing a risk of infection.
The breather pouches used to package the sterile kits may have open or weak seals. This could allow contaminants to enter the kits during medical procedures, increasing the risk of infection for patients and healthcare workers.
Healthcare professionals using Medline dental convenience kits with the listed model numbers and lot numbers from 2024 are most at risk. Patients receiving procedures using these kits could also be affected.
Check for model numbers: DYNJ84880, DYNJ56229A, PHS807626F, DYNJ41929D, DYNJ51841C, or DYNJ905551C. These kits were sold with specific lot numbers from 2024.
Identify the model number on the kit packaging to see if it matches the recalled models listed in the notice.
Reach out to Medline customer service for assistance with returning or replacing the affected kits.
The recall indicates a potential risk of weak seals on breather pouches, so they should not be used until replaced or repaired.
Check the model number on the kit packaging; affected models include DYNJ84880, DYNJ56229A, PHS807626F, DYNJ41929D, DYNJ51841C, and DYNJ905551C with specific 2024 lot numbers.
Contact Medline customer service to return or replace the kit with a safe alternative.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1595-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1595-2025 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.
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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.
