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AAP Implantate Ag recalls aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00
Recalled April 15, 2020 · FDA recall Z-1675-2020 · AAP Implantate Ag
Hazard
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. · FDA Class II
Units
7 units
Sold at
Worldwide Distribution
Description
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.
Product
aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00
Manufacturer(s)
AAP Implantate Ag
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →