The Recall Desk

FDA (Devices) recall action 74835

The Anspach Effort, Inc. recalled 2 products on 2016-10-05

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2016-10-05
Critical
1
Units
—

Why these products were recalled

There was a potential for the Adaptor and Light Adaptor for Small Battery Drive and Small Battery Drive II to generate excessive internal pressure that may cause the products to burst.

The agency’s own wording, quoted from the enforcement report.

1–2 of 2

  • HighFDA (Devices)··2016-10-05

    Anspach Effort Recalls Small Battery Drive Adaptors Due to Burst Risk

    The Anspach Effort, Inc. is recalling 1,833 Small Battery Drive adaptors worldwide because they may generate excessive internal pressure and burst.

    Product
    Adaptor for Small Battery Drive and Small Battery Drive II. Product Usage: The Light Adaptor for Small Battery Drive (SBD) /Small Battery Drive II (SBD II) is designed for use in traumatology and orthopedic surgery of the skeleton, i.e. drilling, reaming or cutting bone. The
    Category
    Distribution
    0 states
  • CriticalFDA (Devices)··2016-10-05

    Anspach Effort Recalls Light Adaptors for Small Battery Drive Devices

    The Anspach Effort, Inc. is recalling Light Adaptors for Small Battery Drive and Small Battery Drive II devices due to a potential risk of bursting from excessive internal pressure.

    Product
    Light Adaptor for Small Battery Drive and Small Battery Drive II.
    Category
    Distribution
    0 states