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VacuBag
Bard Access Systems, Inc. · Model NDB1000 · UDI-DI 00801741036873
EXF
Prescription
9
510(k) clearances
15
Adverse events
3
Recalls
33
Facilities
Description
VacuBag
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-11-03 | Remington Medical, Inc. | There is an error with the "Use by Date" and "Date of Manufacturer" on the box label. |
| 2011-01-12 | Remington Medical Inc. | There have been complaints of the Drainage Bags leaking from the outlet and the inlet port. |
| 2007-07-23 | Remington Medical Inc. | Sterility, inadequate -- Pathway may not be sterile as labeled. |
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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.