FDA recall record

Cardinal Health 200 Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drain,19FR recall — FDA Z-2131-2017

Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased…

Class IIclassification
Z-2131-2017official record ID
May 31, 2017report date

Recall record at a glance

Official recordZ-2131-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCardinal Health 200, LLC
Report dateMay 31, 2017
Recall initiation dateApr 21, 2017
LocationWaukegan, IL, United States

Official product description

Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drain,19FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a radio-opaque section of tubing which has perforations or ducts. The wound drain is surgically placed in a surgical wound site using a trocar. Blood and fluids are collected through a wound drain into a fluid collection reservoir. Wound drains are used to remove exudates from wound sites. Trocars, drains and reservoirs are for a single patient use only and should be discarded after use

Why the product was recalled

Product's seal possibly compromised, potentially compromising the sterility of the package contents. Use of impacted products could result in an increased risk of infection.

Distribution information

Nationwide Distribution

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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