Medline recalls specific procedure kits with plastic syringes that may leak or break, posing health risks during medical use. Affected kits include abdominal hysterectomy and vaginal harper packs with specific pack numbers and lot codes.
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 certain procedure kits that contain plastic syringes prone to leaking or breaking. This could lead to patient health risks during medical procedures if the kits are used as intended.
The plastic syringes in these kits can leak or break, which may cause contamination or injury to patients during medical procedures. This risk is linked to FDA safety alerts about quality issues in the kits.
Healthcare professionals using the recalled procedure kits are most at risk. Patients receiving procedures with these kits may also face health hazards due to potential leaks or breakage.
Check for kits labeled as CSMC/ABDOMINAL HYST PACK-LF, MAJOR VAGINAL HARPER, ROBOT LAP TOTAL HYST, VAG HYSTE PACK-LF, or VAG HYSTERECTOMY PACK-LF with specific pack numbers and lot codes listed in the recall notice.
Look for the specific product names and pack numbers listed in the recall notice to confirm if your kit is affected.
The recall states that these kits may leak or break, posing a risk to patient health. They should not be used until the recall is addressed.
The recall does not specify a remedy, so contact Medline directly for guidance on next steps.
Check the product labels for the specific names and pack 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-1449-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1449-2025 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.
