Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B
Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B was recalled because 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.. If you have this product, stop using it until you verify your lot or model details.
By RecallRadar Editorial Team
Sourced from FDA. Last verified March 15, 2026.
On this page
Free checker
Check if you qualify
See whether your device may qualify for a free repair or replacement program before you spend money.
Check if you qualifyKey facts
- Date announced
- February 18, 2026
- Source agency
- FDA
This recall involves safety concerns. Take action promptly.
✨ Plain-English Summary
Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B was recalled because 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.. If you have this product, stop using it until you verify your lot or model details.
Is This Recall Still Active?
Status: Yes - Active
This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.
What's Being Recalled
Quoted source excerpt from the official notice.
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.
Quick Info
Key facts from the official notice, kept in the article flow for easy cross-checking.
- Brand
- Medline industries, lp
- Category
- medical
- Source agency
- FDA
- Announced
- February 18, 2026
- Country
- US
- Status
- Active
Who's Affected
Specific models and identifiers listed in the source notice:
Model #1
Kit lots 25IBC172 25HBJ413 UDI (ea) 10198459480317 UDI (case) 40198459480318
| # | Model |
|---|---|
| 1 | Kit lots 25IBC172 25HBJ413 UDI (ea) 10198459480317 UDI (case) 40198459480318 |
Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.
What You Should Do
Follow the remedy path from the official notice using the exact model and serial details above.
- 1Stop using the affected product until you verify whether your item is impacted.
- 2Check the official recall notice and match your model, lot, or serial details.
- 3Follow the official instructions for repair, replacement, refund, or disposal.
Source & Verification
This page summarizes the official notice and keeps key facts easy to verify.
- Official source
- FDA
- Announced by source
- February 18, 2026
- Last reviewed by RecallRadar
- March 15, 2026
Frequently Asked Questions
Am I affected by this recall?
Check the affected models section on this page. The official notice currently lists Kit lots 25IBC172 25HBJ413 UDI (ea) 10198459480317 UDI (case) 40198459480318.
What is the remedy for this recall?
Follow the official instructions for repair, replacement, refund, or disposal on the medline industries, lp recall page.
Where can I verify recall details?
Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/device/enforcement.json?search=recall_number:Z-1313-2026&limit=1
Keep browsing with these internal hubs: medline industries, lp recall hub and Medical recall hub.
Official Resources
Use these primary sources for final eligibility and claim instructions.
View official notice from FDASee an inaccuracy?
Help us improve the accuracy of this recall information.
On this page
Free checker
Check if you qualify
See whether your device may qualify for a free repair or replacement program before you spend money.
Check if you qualifyKey facts
- Date announced
- February 18, 2026
- Source agency
- FDA
Related Recalls
Rapid Refill Continuous Injection System, UPN M00566001
Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the manifold, resulting in loose connection or complete disconnection. May lead to difficulty connecting syringe, inability to aspirate or inject properly, fluid leakage, or separation of the syringe from the system, potentially requiring device exchange and prolonging the procedure.
Jul 22, 2026
Papablic Replacement Brush Heads. Model Number: Papablic18B
Potential for brush heads to break.
Jul 22, 2026
Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
Jul 22, 2026
Papablic Replacement Brush Heads. Model Number: PAPA317AA.
Potential for brush heads to break.
Jul 22, 2026
ABIOMED Impella CP Set, Pump Set Code 0048-0003, containing BIOMED Impella Introducer, 14 Fr, 13 cm & 25 cm, Product Code 0052-3046. heart pump and accessories
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
Jul 22, 2026