The Recall Desk

Manufacturer

U&I CORP.

2 recalls in our database name U&I CORP. as the manufacturing or recalling firm.

What the numbers show

Total
2
Critical
0
Severe
0
Most recent
2020-07-29

Of the 2 recalls from U&I CORP. 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.

1–2 of 2

  • ModerateFDA (Devices)·Z-2672-2020·2020-07-29

    U&I Corp Recalls ANAX 5.5 Poly-Reduction Screws Due to Incorrect Laser Etching

    U&I Corp. is recalling six ANAX 5.5 Poly-Reduction Screws because they were laser etched with the wrong size (6.0x45 instead of 6.0x50).

    Product
    ANAX 5.5 Poly-Reduction Screw 6.0X50MM, REF: SFNA6050R, part of ANAX 5.5 SPINAL SYSTEM
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1823-2020·2020-05-06

    U&I Corp. Recalls Velofix SA Cervical Cages Due to Dimensional Defects

    U&I Corp. is recalling 42 Velofix SA cervical cages because screw-hole dimensions may be out of range, posing a risk of screw pullout or instability.

    Product
    Velofix SA cervical cage, REF: TSA161207, TSA161208, TSA161209, TSA161210, TSA161407, TSA161408, TSA161409, TSA161410 - Product Usage:The device is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disk disease at one level fr
    Category
    Medical Device
    Distribution
    Distributed nationwide