AAP Implantate Ag: Medical Device Recall in 2020 - (Recall #: Z-1675-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00

Product Classification:

Class II

Date Initiated: November 28, 2019

Date Posted: April 15, 2020

Recall Number: Z-1675-2020

Event ID: 84716

Reason for Recall:

The company has become aware that the soft tissue retractor is not always removed during the sawing process. This can result in damage to the soft tissue retractor in which abrasion debris can develop and remain in vivo.

Status: Terminated

Product Quantity: 7 units

Code Information:

Lot Numbers: I012, I025, I028

Distribution Pattern:

Worldwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated