FDA-Device2020-04-15Class II
aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00
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.
Sold states
Worldwide Distribution
Affected count
7 units
Manufactured in
Lorenzweg 5, N/A, Berlin, N/A, Germany
Products
aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1675-2020Don't want to check this manually?
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