Medline recalls adult intubation trays with suction catheter kits (SKU DYNJAA245B) that may contain 8Fr instead of 14Fr catheters, risking airway obstruction and respiratory failure.
A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.
Medline is recalling adult intubation trays with suction catheter kits that might include a smaller 8Fr catheter instead of the required 14Fr catheter. Using the wrong size could block the airway, causing breathing problems, emergency treatment, or death.
The recalled kit may contain an 8Fr suction catheter instead of the required 14Fr catheter. This smaller catheter can cause partial or full airway obstruction, leading to hypoxia, respiratory failure, or death if not corrected immediately.
Healthcare professionals using the recalled intubation trays with suction catheter kits (SKU D: DYNJAA245B) are affected. Those performing intubation procedures are most at risk due to potential airway obstruction.
Check for the SKU DYNJAA245B on the intubation tray. The kit was sold with specific lot numbers: 25IBC172 and 25HBJ413. The unique identifiers are UDI (ea) 10198459480317 and UDI (case) 40198459480318.
Immediately stop using the recalled intubation tray with suction catheter kits (SKU DYNJAA245B) to prevent airway obstruction risks.
The recalled kit may contain an 8Fr suction catheter instead of the required 14Fr catheter, which can cause airway obstruction.
Check for SKU DYNJAA245B on the tray and lot numbers 25IBC172 or 25HBJ413.
Stop using it immediately and 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-1313-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1313-2026 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.
