---
title: "DSAART LLC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search DSAART LLC recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/dsaart-llc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# DSAART LLC recall records

**6** reported ongoing

6 records in this archive. Latest source date Sep 26, 2025.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

Sep 26, 2025 FDA device enforcement

### [Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant Model/Catalog Numbers: 600-601 - Silicone Carving Implant Style 6 Size 1 UDI-DI code: B490600601...](https://isitonrecall.com/recall/fda-device-z-0944-2026-brand-name-aart-silicone-carving-implant-product-name-silicone-carving-implant-model-catalog-numbers/)

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

Class II Reported ongoing

Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, PR, TX, UT, VA, WA, and WI O.U.S.: N/A

[Official source for Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant Model/Catalog Nu...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0944-2026%22)

Sep 26, 2025 FDA device enforcement

### [Brand Name: AART Gluteal Implant Product Name: Gluteal Implant Model/Catalog Numbers: 501-101 - Gluteal Implant style 1 size 1 UDI-DI code: B490501101 501-103 - Gluteal Implant ...](https://isitonrecall.com/recall/fda-device-z-0945-2026-brand-name-aart-gluteal-implant-product-name-gluteal-implant-model-catalog-numbers-501-101-gluteal-i/)

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

Class II Reported ongoing

Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, PR, TX, UT, VA, WA, and WI O.U.S.: N/A

[Official source for Brand Name: AART Gluteal Implant Product Name: Gluteal Implant Model/Catalog Numbers: 501-101 - G...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0945-2026%22)

Sep 26, 2025 FDA device enforcement

### [Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog Numbers: 400-0101 Chin Implant style 1 size 1 UDI-DI code: B490400101 400-0103 Chin Implant style 1 size 3...](https://isitonrecall.com/recall/fda-device-z-0946-2026-brand-name-aart-chin-implant-product-name-chin-implant-model-catalog-numbers-400-0101-chin-implant-s/)

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

Class II Reported ongoing

Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, PR, TX, UT, VA, WA, and WI O.U.S.: N/A

[Official source for Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog Numbers: 400-0101 Chin Imp...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0946-2026%22)

Sep 26, 2025 FDA device enforcement

### [Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog Number: 401-202-5 Malar Implant style 2 size 2 left UDI-DI code: B4904012025 401-202-6 Malar Implant sty...](https://isitonrecall.com/recall/fda-device-z-0947-2026-brand-name-aart-malar-implant-product-name-malar-implant-model-catalog-number-401-202-5-malar-implan/)

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

Class II Reported ongoing

Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, PR, TX, UT, VA, WA, and WI O.U.S.: N/A

[Official source for Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog Number: 401-202-5 Malar ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0947-2026%22)

Sep 26, 2025 FDA device enforcement

### [Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/Catalog Number: 500-106-5 Pectoral Implant style 1 size 6 left UDI-DI code: B4905001065 500-106-6 Pectoral...](https://isitonrecall.com/recall/fda-device-z-0948-2026-brand-name-aart-pectoral-implant-product-name-pectoral-implant-model-catalog-number-500-106-5-pector/)

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

Class II Reported ongoing

Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, PR, TX, UT, VA, WA, and WI O.U.S.: N/A

[Official source for Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/Catalog Number: 500-106-5 ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0948-2026%22)

Sep 26, 2025 FDA device enforcement

### [Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number: 502-103 - Calf Implant style 1 size 3 UDI-DI code: B490502103 502-104 - Calf Implant style 1 size ...](https://isitonrecall.com/recall/fda-device-z-0949-2026-brand-name-aart-calf-implant-product-name-calf-implant-model-catalog-number-502-103-calf-implant-sty/)

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

Class II Reported ongoing

Distribution: U.S.: AR, AZ, CA, CO, CT, DC, FL, GA, KY, IL, MA, MD, MI, MN, MS, NE, NJ, NY, OH, OK, PA, PR, TX, UT, VA, WA, and WI O.U.S.: N/A

[Official source for Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number: 502-103 - Calf Imp...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0949-2026%22)

## Reasons in these listed records

- Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

These examples come from this result page and are not a ranking of every recall reason.

## Checking DSAART LLC

### Is there a recall on dsaart llc right now?

This archive contains 6 records, including 6 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search DSAART LLC](https://isitonrecall.com/check/?q=DSAART%20LLC) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
