FDA recall record

C.R. Bard Bard Clean-Cath Intermittent Catheter, 12 French female length recall — FDA Z-1431-2021

The device catheter tip was cut off (no tip) and the product packaging was not fully sealed.

Class IIclassification
Z-1431-2021official record ID
Apr 28, 2021report date

Recall record at a glance

Official recordZ-1431-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmC.R. Bard, Inc.
Report dateApr 28, 2021
Recall initiation dateJan 11, 2021
Quantity9,800 Units
LocationCovington, GA, United States

Official product description

Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only.

Why the product was recalled

The device catheter tip was cut off (no tip) and the product packaging was not fully sealed.

Distribution information

Worldwide distribution - US Nationwide distribution and the countries of Australia, Canada.

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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