AAP Implantate Ag: Medical Device Recall in 2019 - (Recall #: Z-1019-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended for multiple use.

Product Classification:

Class II

Date Initiated: January 11, 2019

Date Posted: March 27, 2019

Recall Number: Z-1019-2019

Event ID: 82159

Reason for Recall:

There is the potential for the Lambotte chisel to break at the welded piece parts of the chisel body and knocking plate.

Status: Terminated

Product Quantity: 25 units

Code Information:

Lot Numbers: I011, I012, I013, I014, I015, I016, I017

Distribution Pattern:

Worldwide Distribution - US Nationwide in the state of Texas and country of Germany

Voluntary or Mandated:

Voluntary: Firm initiated