Medline recalls two convenience kits for potential patient health risks from plastic syringe leaks, breakage, and quality issues. Affected kits include specific pack numbers and lot dates.
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 two medical convenience kits that contain plastic syringes with potential leaks, breakage, or quality issues that could harm patients. This recall is important because medical devices must be safe to prevent patient injury.
The plastic syringes in these kits can leak or break, which may lead to patient health risks. This issue is linked to a recent FDA safety alert about quality problems with similar medical devices.
Healthcare professionals and patients using these kits for medical procedures are most at risk. The kits are used in clinical settings where patient safety is critical.
Check for the specific pack numbers: DYNDA1894 (Lot Numbers 2019080890 or 2019082190) or MNS9580 (Lot Number 2019080890). These kits are labeled as Tracheotomy Tray or Ultrasound Guided PIV Kit.
Look for the pack numbers and lot dates listed in the recall notice to confirm if your kit is affected.
The recall is due to plastic syringes in the kits that may leak or break, posing a risk to patient health as identified by the FDA Safety Alert from March 19, 2024.
The official recall notice does not specify a remedy or action steps beyond checking the labels for affected pack numbers and lot dates.
Yes, affected kits include Tracheotomy Tray with Pack Number DYNDA1894 (Lot Numbers 2019080890 or 2019082190) and Ultrasound Guided PIV Kit with Pack Number MNS9580 (Lot Number 2019080890).
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2981-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2981-2024 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.
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.
