Medline medical convenience kits with specific neonatal intubation trays and resuscitation kits containing recalled endotracheal tubes. These kits pose a risk of serious injury during medical procedures.
Specific Medline Kits were manufactured using Intubation ORAL/NASAL Endotracheal Tubes which were subsequently recalled by Smiths Medical.
Medline has recalled specific neonatal intubation trays and newborn resuscitation kits because they contain endotracheal tubes previously recalled by Smiths Medical. These kits are used in hospitals for infant medical emergencies and could cause serious injury if used improperly.
The endotracheal tubes in these kits were manufactured using tubes that were previously recalled by Smiths Medical as unsafe. This could lead to serious injury during infant intubation procedures if the tubes fail or cause complications.
Healthcare providers using Medline neonatal intubation trays or newborn resuscitation kits with the listed model numbers and lot numbers are affected. Newborns in hospitals using these kits are at the highest risk.
Check for model numbers: ACC010371C, ACC010381A, ACC010381B, ACC010381C, ACC010395, ACC010397, ACC010541A, ACC010541B, ACC010541C, or DYNJAA252. Look for specific lot numbers listed in the recall notice.
Identify the model number on your Medline kit to see if it matches the recalled list.
Reach out to Medline directly for assistance with the recall process.
These kits contain endotracheal tubes that were previously recalled by Smiths Medical as unsafe, which could cause serious injury during infant intubation procedures.
No, but you should check if your kit is affected and contact Medline for guidance.
Check the model number and lot numbers against the list provided in the recall notice, then contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1505-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1505-2025 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.
