FDA recall record

C.R. Bard Bard Nasogastric Sump Tube and PreVent Anti-Reflux Filter and Lopez Valve with recall — FDA Z-0802-2024

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction,…

Class IIclassification
Z-0802-2024official record ID
Jan 31, 2024report date

Recall record at a glance

Official recordZ-0802-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmC.R. Bard Inc.
Report dateJan 31, 2024
Recall initiation dateDec 20, 2023
Quantity3360 units
LocationCovington, GA, United States

Official product description

Bard Nasogastric Sump Tube and PreVent Anti-Reflux Filter and Lopez Valve with ENFit, 12Fr., 48in Long, REF EN0056120

Why the product was recalled

BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.

Distribution information

US

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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