The Recall Desk

Manufacturer

Allergan Inc

3 recalls in our database name Allergan Inc as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
0
Most recent
2015-07-29

Of the 3 recalls from Allergan Inc 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.

1–3 of 3

  • ModerateFDA (Devices)·Z-2104-2015·2015-07-29

    Allergan Recalls Natrelle Tissue Expanders for Expired Shelf Life

    Allergan is recalling Natrelle CUI Series Tissue Expanders because the shipped products were beyond their shelf life. The recall involves 23 units total, with 16 distributed in the US.

    Product
    Natrelle CUI Series Tissue Expanders. Product Usage: Natrelle CUI Series Tissue Expander has been designed for temporary implantation to develop a skin flap. The device is used for reconstructive correction of a defect or to provide cover for a prosthetic implant. The CUI Tis
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2103-2015·2015-07-29

    Allergan Recalls Natrelle Tissue Expanders Due to Expired Shelf Life

    Allergan is recalling Natrelle 133 and CUI Series Tissue Expanders because the shipped products were beyond their 47-month shelf life.

    Product
    Natrelle 133 Series Tissue Expanders Product Usage: Natrelle 133 Series Tissue Expander is intended for temporary subcutaneous implantation and require periodic, incremental inflation with sterile saline for injection until the desired amount of tissue is developed.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1988-2015·2015-07-15

    Allergan Recalls Expired Natrelle Breast Implant Sizers

    Allergan is recalling 9 units of expired Natrelle 410cc Re-Sterilizable Breast Implant Sizers because they were shipped to the user level.

    Product
    Natrelle Re-sterilizable Breast Implant Sizer, Size: 410 cc, Style No. MSZFX410. The product is packaged in a thermoformed tray (double sterile barrier) and enclosed in a labeled carton.
    Category
    Medical Device
    Distribution
    5 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.

Allergan, Inc.

U.S. subsidary of Allergan plc

Country
United States
Founded
1950
Parent company
Allergan plc

Official website

Source: Wikidata (Q505866), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.