# FDA recall Z-1078-2024

> **Zimmer Surgical Inc** · Class II · device recall initiated 2024-01-02.

## Product

3:1 Dermacarrier, Model Number 00219501300, skin graft carrier

## Reason for recall

Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The problem may lead to minor tissue damage or additional unplanned graft if deemed necessary.

## Distribution

Worldwide - US Nationwide distribution including in the states of CA, DE, FL, GA, IA, IL,  IN, KS, LA, MI, MO, MT, NC, NV, NY, OH, OK, PA, RI, TN, TX, UT, VA, WA, WI, WV and the countries of AUTRALIA, CANADA, DNIPRO OBLAS, HONG KONG, INDIA, JAPAN, MEXICO,  CDMX, NETHERLANDS, SEOUL KOREA, SINGAPORE, TAIWAN, THAILAND.

## Key facts

- **Recall number:** Z-1078-2024
- **Recalling firm:** Zimmer Surgical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-02
- **Report date:** 2024-02-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dover, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1078-2024

## Citation

> AI Analytics. FDA recall Z-1078-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1078-2024. Source: US FDA. Licensed CC0.

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