FDA recall record

Halyard Health KimVent Wet Pak, Closed Suction System for Adults, Double Swivel Elbow, 14 Fr recall — FDA Z-1222-2015

Defect: A hole or crack was found which may cause air to leak.

Class IIclassification
Z-1222-2015official record ID
Mar 11, 2015report date

Recall record at a glance

Official recordZ-1222-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHalyard Health
Report dateMar 11, 2015
Recall initiation dateJan 16, 2015
Quantity83 cases (20 tubes per case)
LocationRoswell, GA, United States

Official product description

KimVent Wet Pak, Closed Suction System for Adults, Double Swivel Elbow, 14 Fr. Sterile, Distributed by Kimberly Clark Global Systems, LLC.

Why the product was recalled

Defect: A hole or crack was found which may cause air to leak.

Distribution information

CA, FL, IL, LA, MA, MK, MN, MS, NM, NY, OK and TX and Japan.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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