Medline ClearPro Trach T-Piece Suction Catheter Recall: Risk of Disassembly During Use
Medline recalls ClearPro Trach T-Piece Closed Suction Catheter Model DYNCPTP14T due to reports of the catheter coming apart during use, which could cause injury. Affected patients should contact Medline for details.
Use caution until it’s fixed
There are reports of the suction catheter coming apart from the device assembly during use.
Contact the company
What happened, in plain English
Medline is recalling a specific trach suction catheter model because it has been reported to come apart during use. This could lead to injury if the catheter breaks while being used on a patient with a tracheostomy tube. Read more at govinfonow.com/recall/64881-medline-clearpro-trach-t-piece-suction-catheter-recall-risk-of.
Source Summary by GovInfoNow · govinfonow.com/recall/64881-medline-clearpro-trach-t-piece-suction-catheter-recall-risk-of · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2725-2020
Cite this page
“Medline ClearPro Trach T-Piece Suction Catheter Recall: Risk of Disassembly During Use.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64881-medline-clearpro-trach-t-piece-suction-catheter-recall-risk-of. Based on FDA recall #Z-2725-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2725-2020%22&limit=1).
Why it’s dangerous
The catheter can come apart during use, which may cause injury to the patient. This is a risk during the suction process for patients with artificial airways.
Who’s affected
Patients using this catheter for tracheostomy tube suction are most at risk. Healthcare providers who use this model for endotracheal suction in adults are also affected.
How to tell if you have this one
Check for the model number DYNCPTP14T on the catheter. The product was sold with lot number 6918100021.
- Brand
Medline- Category
Medical device
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution including in the states of AR, AZ, CA, FL, GA, IL, MS, NY, NV, OH, PA, TX.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2724-2020 | ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.; Model: DYNCPTP14, Lot #6919020016: | 2440 units |
| Z-2725-2020 | ClearPro Trach T-Piece Closed Suction Catheter, Model DYNCPTP14T, 14 Fr 12.5 IN FOR TRACHEOSTOMY TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.; Model: DYNCPTP14T, Lot #6918100021: | 680 units |
What to do — step by step
Check Product Details
Look for the model number DYNCPTP14T and lot number 6918100021 on the catheter.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 12 states.
FDA distribution: “US Nationwide distribution including in the states of AR, AZ, CA, FL, GA, IL, MS, NY, NV, OH, PA, TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, Arkansas, California, Florida, Georgia, Illinois, Mississippi, Nevada, New York, Ohio, Pennsylvania, Texas.
Recall timeline
FDA published this recall 36 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-2725-2020 (June 30, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2725-2020 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.