The Recall Desk

Manufacturer

Signature Orthopedics Pty Limited

4 recalls in our database name Signature Orthopedics Pty Limited as the manufacturing or recalling firm.

What the numbers show

Total
4
Critical
0
Severe
0
Most recent
2021-06-09

Of the 4 recalls from Signature Orthopedics Pty Limited 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.

1–4 of 4

  • HighFDA (Devices)·Z-1694-2021·2021-06-09

    Hip implant cup liner recalled for mislabeling and wrong product in package

    Signature Orthopedics is recalling Logical cup liners (hip implants) due to mislabeling with incorrect products in the package. Affected devices may not be suitable for implantation.

    Product
    Logical cup liner - Product Usage: intended to replace a hip joint where bone stock is sufficient to support the implant.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0834-2019·2019-02-20

    Signature Orthopedics Recalls Three Genius Knee Cemented CR Femoral Components

    Signature Orthopedics is voluntarily recalling three Genius Knee Cemented CR Femoral Components due to a product mix-up. The devices were distributed in Florida, New York, and Tennessee.

    Product
    Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement component
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0833-2019·2019-02-20

    Signature Orthopedics Recalls Genius Knee Cemented Tibial Components Due to Product Mix-Up

    Signature Orthopedics is recalling 10 Genius Knee Cemented Tibial Components due to a product mix-up. The recall covers units distributed in Florida, New York, and Tennessee.

    Product
    Genius Knee Cemented Tibial Component Product Usage: Knee replacement component
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0920-2018·2018-03-14

    Signature Ceramic Femoral Head Recalled for Mislabeled Packaging

    Signature Orthopedics is recalling 10 ceramic femoral heads because the packaging labels do not match the component sizes, which may cause surgical delays.

    Product
    Signature Ceramic Femoral Head. Model Number: 111-152-621. The Signature ceramic femoral heads are manufactured by Ceramtec from 72-75% Al2O3+24-26% Z3O3 (Biolox Delta). The heads connect via a 12/14 taper to the stem trunnion, and articulates against the crosslinked UHMWPE lin
    Category
    Medical Device
    Distribution
    Distributed nationwide