The Recall Desk

Manufacturer

The Metrix Company

33 recalls in our database name The Metrix Company as the manufacturing or recalling firm.

What the numbers show

Total
33
Critical
0
Severe
0
Most recent
2024-11-20

Of the 33 recalls from The Metrix Company 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.

26–33 of 33

  • HighFDA (Devices)·Z-2260-2016·2016-08-03

    Metrix Container Fill and Transfer Sets Recalled for Dispensing Accuracy Issues

    The Metrix Company is recalling container fill and transfer sets because they cannot meet designed accuracy specifications when dispensing into bags.

    Product
    Container fill and transfer sets, 250 mL, 500 mL, 1000 mL, 2000 mL, 3000 mL, or 4000 mL.
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-2261-2016·2016-08-03

    Metrix Container Fill and Transfer Sets Recalled for Dispensing Accuracy Issues

    The Metrix Company is recalling container fill and transfer sets because they may not meet designed accuracy specifications when dispensing into bags.

    Product
    Container fill and transfer sets, automatic fill compatible, 250 mL, 500 mL, 1000 mL, 1500 mL, 2000 mL, 3000 mL, or 4000 mL.
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-2264-2016·2016-08-03

    Metrix Container Fill and Transfer Sets Recalled for Dispensing Accuracy Issues

    The Metrix Company is recalling 250 mL and 500 mL container fill and transfer sets because the associated auto compounding device cannot meet designed accuracy specifications when dispensing into bags.

    Product
    Container fill and transfer sets, 250 mL and 500 mL, . .
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-2262-2016·2016-08-03

    Metrix Dual Chamber Container Fill and Transfer Sets Recalled for Accuracy Issues

    The Metrix Company is recalling Dual Chamber Container fill and transfer sets because the associated auto compounding device cannot meet designed accuracy specifications for dispensing volume.

    Product
    Dual Chamber Container fill and transfer sets, 250 mL / 1250 mL or 500 mL / 2500 mL
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-2263-2016·2016-08-03

    Metrix Dual Chamber Container Recall Due to Dispensing Accuracy Issues

    The Metrix Company is recalling Dual Chamber Containers because the associated auto-compounding device cannot meet accuracy specifications when dispensing into the bags.

    Product
    Dual Chamber Container fill with gravity/attached transfer sets, 250 mL / 1250 mL, 300 mL / 1700 mL, 500 mL / 2500 mL, 500 mL / 3500 mL
    Category
    Medical Device
    Distribution
    21 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.

Metrix

Country
Belgium
Founded
2004

Source: Wikidata (Q110412412), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.