Home › C. R. Bard, Inc. › Bard® Nasogastric Sump Tube
Bard® Nasogastric Sump Tube
C. R. Bard, Inc. · Model 0042140 · UDI-DI 00801741052255
BSS
Prescription
10
510(k) clearances
198
Adverse events (10 deaths)
5
Recalls
11
Facilities
Description
Bard® Nasogastric Sump Tube
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-20 | C.R. Bard Inc | 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 occ |
| 2023-12-20 | C.R. Bard Inc | 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 occ |
| 2023-12-20 | C.R. Bard Inc | 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 occ |
| 2023-12-20 | C.R. Bard Inc | 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 occ |
| 2023-12-20 | C.R. Bard Inc | 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 occ |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.