The Recall Desk

Manufacturer

ReFlow Medical

1 recall in our database name ReFlow Medical as the manufacturing or recalling firm.

What the numbers show

Total
1
Critical
0
Severe
0
Most recent
2017-05-24

Of the 1 recalls from ReFlow Medical 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 listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–1 of 1

  • HighFDA (Devices)·Z-1898-2017·2017-05-24

    ReFlow Medical Recalls Wingman 35 Crossing Catheters Due to Tip Detachment Risk

    ReFlow Medical is recalling Wingman 35 Crossing Catheters because they may be prone to tip detachment. The recall affects 2,794 units distributed in the US and internationally.

    Product
    Wingman 35 Crossing Catheter, 65cm, Model Numbers: WGM35065US WGM35065CE WGM35090US WGM35090CE WGM35135US WGM35135CE
    Category
    Medical Device
    Distribution
    Distributed nationwide