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.
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