PlainRecalls
FDA Devices Moderate Class II Ongoing

Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 18Fr., 48in Long, REF EN0056180

Reported: January 31, 2024 Initiated: December 20, 2023 #Z-0805-2024

Product Description

Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 18Fr., 48in Long, REF EN0056180

Reason for Recall

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.

Details

Recalling Firm
C.R. Bard Inc
Units Affected
9860 units
Distribution
US
Location
Covington, GA

Frequently Asked Questions

What product was recalled?
Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 18Fr., 48in Long, REF EN0056180. Recalled by C.R. Bard Inc. Units affected: 9860 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 31, 2024. Severity: Moderate. Recall number: Z-0805-2024.