Medline recalls 14 types of tracheostomy kits with plastic syringes that may leak or break, posing health risks. Affected kits include specific pack and lot numbers listed in the recall.
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 14 different tracheostomy convenience kits because their plastic syringes can leak or break, which may harm patients. These kits are used in medical settings and contain specific pack and lot numbers that are listed in the recall.
The plastic syringes in these kits have been identified by the FDA as having leaks and breakage issues. This can lead to potential harm to patients during medical procedures, such as infections or injuries from broken syringes.
Healthcare providers and medical facilities that use these kits are most at risk. Patients using the recalled kits could face health issues if the syringes leak or break.
Check for the product names listed: Tracheotomy tray, Tracheostomy, or Trach pack kits with specific pack numbers (e.g., DYNDA1894, DYNJ45495G) and lot numbers (e.g., 21HBD322, 21KBO731).
Look for the pack number and lot number on the kit to confirm if it's affected. Affected kits include specific pack numbers like DYNDA1894 and lot numbers such as 21HBD322.
The FDA identified leaks and breakage issues in the plastic syringes of these kits, which could pose a risk to patient health.
Check the pack number and lot number on the kit. Affected kits include specific pack numbers like DYNDA1894 and lot numbers such as 21HBD322.
The recall does not specify a remedy, so contact Medline directly for guidance on how to handle affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2984-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2984-2024 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.
