FDA Device Intelligence
HomeDevice types › KDQ

Bottle, Collection, Vacuum

FDA product code KDQ · Class 2 · General Hospital

923
Registered devices
2,074
Adverse events
33
Recalls
48
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-06-27MEDLINE INDUSTRIES, LP - NorthfieldDue to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/
2024-03-22MEDLINE INDUSTRIES, LP - NorthfieldA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
2024-03-22MEDLINE INDUSTRIES, LP - NorthfieldA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
2024-03-22MEDLINE INDUSTRIES, LP - NorthfieldA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
2024-03-22MEDLINE INDUSTRIES, LP - NorthfieldA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
2024-03-22MEDLINE INDUSTRIES, LP - NorthfieldA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
2024-03-22MEDLINE INDUSTRIES, LP - NorthfieldA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
2024-03-22MEDLINE INDUSTRIES, LP - NorthfieldA slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
2023-09-05Atrium Medical CorporationProduct was re-processed and re-sterilized by a third party using packaging configurations and a sterilization process which are not approved by the manufacture
2023-03-01Atrium Medical CorporationThe Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the Express Mini 500 Dry Seal Chest Drains do not provide sufficient precaution against

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.