Reported Sep 9, 2015 · Terminated
KimVent* Wet Pak* Closed Suction System for Adults, 14 F, T-Piece (Product Code 22056); KimVent* Wet Pak* Closed…
Halyard Health, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Halyard Health, Inc · 5405 Windward Pkwy · Alpharetta, GA · 30004-3894
Is this the product you have?
3 of 3 products
| Model / number | Product as published |
|---|---|
22056 | KimVent* Wet Pak* Closed Suction System for Adults, 14 F, T-Piece ( ) |
22556 | KimVent* Wet Pak* Closed Suction System for Adults, 16 F, T-Piece ( ) |
22012356 | KimVent* Wet Pak* Closed Suction System for Adults, 14 F, T-Piece ( ) A tracheobronchial suction catheter is a device that is attached to a port of the airway circuit for use as needed to aspirate liquids or semisolids from a patient's upper airway. |
- Lot codes and dates
Product Code 22056 - AB5124U18AB5138U01AB5145U02AB5145U05AB5153U03Product Code 22556 - AB5124U07AB5131U04Product Code 22012356 - AB5145U09
- Amount recalled
- N/A
This recall covers 32 products
The agency filed one notice per product. You are reading one of them; the other 31 are below.
19 more are in the archive.
Where it was sold
- Nationwide
- PR
Why it was recalled
The thumb valve of some KIMVENT Closed Suction Systems remained partially open after suctioning was completed, even though the valve appeared to be closed or in the "LOCKED" position.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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