Every recall we track for DSAART LLC — 6 in all — plus the complaints and injury reports the public filed about them.
AART recalls gluteal implants with model numbers 501-101 to 501-310 due to FDA approval issues. Consumers should check UDI-DI codes for affected products.
AART recalls specific pectoral implants due to FDA approval deficiencies. Affected models include 500-106-5 to 500-403-6 with certain lot numbers. Consumers should check UDI-DI codes and contact the manufacturer.
AART recalls chin implants with model numbers 400-0101 to 400-0302 that were distributed without required FDA premarket approvals. Consumers should check their product details to ensure safety.
Recalled AART Silicone Carving Implants (models 600-601 to 600-804) due to FDA approval issues. Check UDI-DI codes and lot numbers for affected items.
AART Malar Implant model 401-202-5 and 401-202-6 were recalled due to FDA approval issues. The products were distributed without required premarket approvals.
AART recalls specific calf implant models (502-103 to 502-304) due to lack of FDA premarket approval. Consumers should check UDI-DI codes and lot numbers for affected items.
