PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: April 15, 2020 Initiated: November 28, 2019 #Z-1675-2020

Product Description

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

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.

Details

Recalling Firm
AAP Implantate Ag
Units Affected
7 units
Distribution
Worldwide Distribution
Location
Berlin, N/A

Frequently Asked Questions

What product was recalled?
aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00. Recalled by AAP Implantate Ag. Units affected: 7 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 15, 2020. Severity: Moderate. Recall number: Z-1675-2020.