# FDA recall Z-1482-2022

> **Aesculap Implant Systems LLC** · Class II · device recall initiated 2020-04-01.

## Product

PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8361-10

## Reason for recall

Endoscopic graspers may become separated at the weld from handle to the shaft of the device.

## Distribution

United States Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY, Washington DC and Puerto Rico.

## Key facts

- **Recall number:** Z-1482-2022
- **Recalling firm:** Aesculap Implant Systems LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2020-04-01
- **Report date:** 2022-08-10

- **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-1482-2022

## Citation

> AI Analytics. FDA recall Z-1482-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1482-2022. Source: US FDA. Licensed CC0.

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