Medline recalls 26 procedural kits with plastic syringes that may leak or break, posing a risk to patient health. Kits labeled with specific pack numbers and lot numbers are affected.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Medline is recalling 26 different procedural kits that contain plastic syringes which may leak or break. This could pose a risk to patient health due to quality issues identified in the FDA safety alert.
The plastic syringes in these kits have been identified as having leaks or breakage issues. These quality problems could lead to potential risks to patient health during medical procedures.
Healthcare professionals and medical facilities that use these procedural kits are most at risk. Patients using these kits during procedures may be affected if the syringes leak or break.
Check for kits labeled with specific pack numbers and lot numbers listed in the recall notice. The affected kits include items like AFCH ANTERIOR SEGMENT PK (Pack Number DYNJ63330B) and others with detailed pack numbers and lot numbers.
Look for specific pack numbers and lot numbers listed in the recall notice to identify affected kits.
The plastic syringes in these kits may leak or break, which could pose a risk to patient health.
The affected kits include 26 specific procedural kits with pack numbers and lot numbers listed in the recall notice.
Check the kit labels for specific pack numbers and lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2765-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2765-2024 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.
