# FDA recall Z-0017-2026

> **S.I.N. Implant System Ltda** · Class II · device recall initiated 2025-07-30.

## Product

IMPLANT EPIKUT PLUS MT16 3,5X10,0MM, REF: ILM 3510N;  IMPLANT EPIKUT PLUS MT16 3.8X11.5MM, REF: ILM 3511N;  IMPLANT EPIKUT PLUS MT16  3,5X13,0MM, REF: ILM 3513N;  IMPLANT EPIKUT PLUS MT16  3,5X15,0MM, REF: ILM 3515N;  IMPLANT EPIKUT PLUS MT16  3,8X10,0MM, REF: ILM 3810N;  IMPLANT CM16  3,8 X 11MM, REF: ILM 3811N;  IMPLANT EPIKUT PLUS MT16  3,8X15,0MM, REF: ILM 3815N;  IMPLANT EPIKUT PLUS MT16  4,0X10,0MM, REF: ILM 4010N;  IMPLANT EPIKUT PLUS MT16  4,0X11,5MM, REF: ILM 4011N;  IMPLANT EPIKUT PLUS MT16  4,0X13,0MM, REF: ILM 4013N;  IMP EPIKUT PLUS LONG MT16  4,0X20,0MM, RES: ILM 4020N;  IMPLANT EPIKUT PLUS MT16  4,0X8,5MM, RES: ILM 4085N;  IMPLANT EPIKUT PLUS MT16  4,5X13,0MM, REF: ILM 4513N;  IMPLANT EPIKUT PLUS MT16  4,5X15,0MM, REF: ILM 4515N;  IMPLANT EPIKUT PLUS MT16  4,5X8,5MM, REF: ILM 4585N;  IMPLANT EPIKUT PLUS MT16  5,0X10,0MM, REF: ILM 5010N;  IMPLANT EPIKUT PLUS MT16  5,0X11,5MM, REF: ILM 5011N;  IMPLANT EPIKUT PLUS MT16  4,5X10,0MM, REF: ILM 4510N;  IMPLANT EPIKUT PLUS MT16 

## Reason for recall

Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging damage, which could compromise product quality and performance.

## Distribution

US Nationwide distribution including in the states of TX, IL, KY, NC, TN, CO, CA, MO, MD, AL, FL, PA, UT, NE, ID, AZ, WA, OK, OR, NV, NJ, VA, NY, LA, CT, SD, SC, HI, KS, MA, MI, NM, OH, MT, WI, MN, ME.

## Key facts

- **Recall number:** Z-0017-2026
- **Recalling firm:** S.I.N. Implant System Ltda
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-30
- **Report date:** 2025-10-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sao Paulo, N/A, Brazil

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0017-2026

## Citation

> AI Analytics. FDA recall Z-0017-2026. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-0017-2026. Source: US FDA. Licensed CC0.

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