Reported Sep 9, 2015 · Terminated
KimVent* Closed Suction System for Adults, 14 F, DSE (Product Code 2210); KimVent* Closed Suction System for Adults, 12…
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?
4 of 4 products
| Model / number | Product as published |
|---|---|
2210 | KimVent* Closed Suction System for Adults, 14 F, DSE ( ) |
| — | KimVent* Closed Suction System for Adults, 12 F, DSE (Product 21603) |
22103 | KimVent* Closed Suction System for Adults, 14 F, DSE ( ) |
22714183 | KimVent* Closed Suction System for Adults, 14 F, DSE ( ) 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 2210 - M5054T630M5082T625M5089T611M5117T627Product Code 21603 - M5089T618M5103T610Product Code 22103 - M5089T617Product Code 22714183 M5082T318
- 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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