DSAART Recalls
6 recalls on record · December 24, 2025 to December 24, 2025 · Medical Devices
December 24, 2025Medical DevicesFDA
DSAART LLC recalls Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number: 502-103 - Calf Implant style 1 size 3
Hazard: Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
December 24, 2025Medical DevicesFDA
DSAART LLC recalls Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/Catalog Number: 500-106-5 Pectoral Implant sty
Hazard: Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
December 24, 2025Medical DevicesFDA
DSAART LLC recalls Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog Number: 401-202-5 Malar Implant style 2 size
Hazard: Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
December 24, 2025Medical DevicesFDA
DSAART LLC recalls Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog Numbers: 400-0101 Chin Implant style 1 size 1
Hazard: Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
December 24, 2025Medical DevicesFDA
DSAART LLC recalls Brand Name: AART Gluteal Implant Product Name: Gluteal Implant Model/Catalog Numbers: 501-101 - Gluteal Implant style
Hazard: Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
December 24, 2025Medical DevicesFDA
DSAART LLC recalls Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant Model/Catalog Numbers: 600-601 - Silico
Hazard: Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.