# FDA recall Z-1485-2026

> **Aesculap Inc** · Class II · device recall initiated 2026-01-15.

## Product

Brand Name: AESCULAP  Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM  Model/Catalog Number: FF399R  Software Version: N/A  Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM  Component: N/A

## Reason for recall

There is the potential for the length of the trocar shaft to be too long.

## Distribution

US Nationwide distribution in the states of AZ, AR, CA, CO, FL, GA, HI, IA, ID, IL, KS, LA, MA, MD, MI, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, RI, SC, SD, TX, UT, WA.

## Key facts

- **Recall number:** Z-1485-2026
- **Recalling firm:** Aesculap Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-15
- **Report date:** 2026-03-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1485-2026

## Citation

> AI Analytics. FDA recall Z-1485-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1485-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*