The Recall Desk

Hazard

Fluid Separation recalls

9 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9
Critical
0
Severe
0
Most recent
2019-11-13

Of the 9 fluid separation recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all fluid separation recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–9 of 9

  • HighFDA (Devices)·Z-0284-2020·2019-11-13

    Becton Dickinson Recalls MaxZero Extension Sets Due to Fluid Separation

    Becton Dickinson is voluntarily recalling MaxZero Extension Sets with Needle-less Connectors because fluid droplets may separate from the sealed surface after disconnection.

    Product
    MaxZero Extension Sets with Needle-less Connector, Product codes MZ1000 MZ1000-07 MZ5301 MZ5302 MZ5303 MZ5304 MZ5305 MZ5306 MZ5307 MZ5309 MZ5310 MZ5312 MZ5313 MZ5316 MZ8001 MZ8002 MZ8003 MZ9266 MZ9267 MZ9272 MZ9273 MZ9274 MZ9275 MZ9276 MZ9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0100-2020·2019-10-16

    Centurion Medical Products Recalls OR VANTEX Kits Due to Connector Defect

    Centurion Medical Products is recalling OR VANTEX kits because the included BD MaxZeroNeedleess Connector may allow fluid droplets to separate after disconnection.

    Product
    OR VANTEX 7FR 3L 16CM CVC ECVC6665
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0089-2020·2019-10-16

    Centurion Medical Recalls Central Venous Access Device Bundles

    Centurion Medical Products Corporation is recalling Central Venous Access Device Bundles because they include a connector recalled for potential fluid droplet separation.

    Product
    CENTRAL VENOUS ACCESS DEVICE BUNDLE ECVC2840
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0080-2020·2019-10-16

    Centurion Medical Recalls Port and IO Access Dressing Kits

    Centurion Medical Products Corporation is recalling Port and IO Access Dressing Kits because they include a connector recalled for potential fluid droplet separation.

    Product
    PORT AND IO ACCESS DRESSING KIT DT15780A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0098-2020·2019-10-16

    Centurion Medical Central Line Bundle Recalled for Fluid Droplet Risk

    Centurion Medical is recalling central line bundles containing a BD MaxZeroNeedleess Connector due to the potential for fluid droplets to separate from the sealed surface after disconnection.

    Product
    CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0085-2020·2019-10-16

    Centurion Medical Recalls Infusa Port Kits Due to Fluid Droplet Risk

    Centurion Medical Products Corporation is recalling Infusa Port Kits containing a specific connector due to the potential for fluid droplets to separate from the sealed surface.

    Product
    INFUSA PORT KIT DYNDC1840F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0079-2020·2019-10-16

    Centurion Medical CVC Bundle Recall Due to Fluid Droplet Risk

    Centurion Medical is recalling CVC bundles containing a recalled BD connector due to potential fluid droplet separation.

    Product
    CVC BUNDLE WITHOUT CATH CVI4600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0084-2020·2019-10-16

    Centurion Infusa Port Kit Recalled for Fluid Droplet Risk

    Centurion Medical Products is recalling Infusa Port Kits containing a recalled BD connector due to the potential for fluid droplets to separate from the sealed surface.

    Product
    INFUSA PORT KIT DYNDC1840E
    Category
    Medical Device
    Distribution
    Distributed nationwide