The Recall Desk

FDA (Devices) recall action 67176

The Anspach Effort, Inc. recalled 2 products on 2014-02-05

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
2014-02-05
Critical
0
Units
628

Why these products were recalled

Cutter was longer than was stated on the label

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

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

1–2 of 2

  • ModerateFDA (Devices)··2014-02-05

    Anspach Recalls Single-Use Sterile Bone Cutting Burs Due to Length Discrepancy

    The Anspach Effort, Inc. is recalling 599 single-use sterile bone cutting burs because the cutters were longer than stated on the label.

    Product
    AnspacSingle use Sterile bone cutting burs.h REF: S-1504TD Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs.
    Category
    Distribution
    6 states
  • ModerateFDA (Devices)··2014-02-05

    Anspach Twist Drill Recall Due to Incorrect Length Labeling

    The Anspach Effort, Inc. is recalling 29 single-use sterile twist drills because the cutters were longer than stated on the label.

    Product
    Anspach REF: TURQ-434-4 Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs.
    Category
    Distribution
    6 states