FDA recall record

Bard Medical Division SureStep(TM) FOLEY TRAY SYSTEM, Preconnected Closed System Foley Tray recall — FDA Z-0803-2019

potential for urine leakage around the vent on the vented sample port

Class IIclassification
Z-0803-2019official record ID
Feb 13, 2019report date

Recall record at a glance

Official recordZ-0803-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBard Medical Division
Report dateFeb 13, 2019
Recall initiation dateDec 13, 2018
Quantity883,171 units
LocationCovington, GA, United States

Official product description

SureStep(TM) FOLEY TRAY SYSTEM, Preconnected Closed System Foley Tray, Product Codes: A119214M, A119216M, A119218M, A119416M, A153200, A300916A, A301216, A301216A, A303314A, A303316A, A303318A, A303414A, A303416A, A303418A, A304400A, A304714A, A304716A, A304718A, A304914, A304916, A304918, A307414A, A307416A, A319414AM, A319416A, A319416AM, A319418AM, A319514AM, A319516A, A319516AM, A333100A, A333416A, A339414AM, A339516AM, A339516AM, A344916, A800064, A800065, A800364, A800365, A800366, A900216, A900416, A901216, A902114, A902216, A902414, A902416, A902418, A902616, A902914, A902916, A902918, A903314A, A903316A, A903318A, A903416A, A904100, A904400A, A909116M, A909216M, A919416AM, A919516AM, A942206, A942208, A942210, A942212, A942214, A942216, A942218, A942616, A942618, A943214, A943216, A943218, MTA902416 Product Usage catheter

Why the product was recalled

potential for urine leakage around the vent on the vented sample port

Distribution information

US, Canada, UAE

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

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About this record

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