The Recall Desk

Manufacturer

Leonhard Lang Gmbh

1 recall in our database name Leonhard Lang Gmbh as the manufacturing or recalling firm.

What the numbers show

Total
1
Critical
0
Severe
0
Most recent
2014-12-31

Of the 1 recalls from Leonhard Lang Gmbh 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.

1–1 of 1

  • HighFDA (Devices)·Z-0802-2015·2014-12-31

    GE Healthcare Pediatric Defibrillation Electrodes Recalled for Arcing Risk

    Leonhard Lang GmbH is recalling GE Healthcare Pediatric Defibrillation Electrodes because arcing may cause malfunction, delaying or preventing life-saving therapy.

    Product
    GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing Electrodes. REF 2059144-001 and 2059144-005. . Product Usage: Usage: Skintact Pediatric Multifunction Electrodes are for use on pediatric patients, less than 8 years of age, or weighing less than 25 kg (
    Category
    Medical Device
    Distribution
    Distributed nationwide