The Recall Desk

Manufacturer

The Seaberg Company Inc

3 recalls in our database name The Seaberg Company Inc as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
3
Most recent
2018-06-20

Of the 3 recalls from The Seaberg Company Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3 (100%) 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.

1–3 of 3

  • SevereFDA (Devices)·Z-2227-2018·2018-06-20

    Seaberg SAM XT-C Tourniquet Recall Due to Potential Buckle Failure

    The Seaberg Company is recalling SAM XT-C tourniquets because internal testing showed stitches securing the buckle might fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-C, Model: Hi-Viz Orange or Civilian
    Category
    Medical Device
    Distribution
    23 states
  • SevereFDA (Devices)·Z-2226-2018·2018-06-20

    Seaberg SAM XT-M Tourniquet Recalled for Potential Buckle Failure

    The Seaberg Company is recalling SAM XT-M tourniquets because internal testing found stitches securing the buckle could fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-M, Model: Tactical Black or Military
    Category
    Medical Device
    Distribution
    23 states
  • SevereFDA (Devices)·Z-2228-2018·2018-06-20

    Seaberg SAM XT-C Tourniquet Recalled for Potential Buckle Stitch Failure

    The Seaberg Company is recalling SAM XT-C tourniquets because internal testing showed stitches securing the buckle could fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-C, Model: Hi-Viz Blue
    Category
    Medical Device
    Distribution
    23 states

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

SEABERG

Czech company

Country
Czech Republic
Founded
2007

Source: Wikidata (Q67811696), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.