# FDA recall Z-1297-2021

> **Stryker Communications** · Class II · device recall initiated 2021-01-29.

## Product

S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502  Components that are affected within the S-Series Finished Good Model Number  o	P38198 - ASM, MFR CONTROLLER, FIXED STANDARD  o	P38199 - ASM, MFR CONTROLLER, LIFT STANDARD  o	P40553 - ASM, MFR HANDLE REPAIR, LIFTING, S-SERIES, STANDARD  o	P40554 - ASM, MFR HANDLE REPAIR, FIXED, S-SERIES, STANDARD  o	P46269 - ASSY, MFR CONTROLLER UPGRADE, STANDARD

## Reason for recall

The manufacturer has become aware that there is a likelihood that the S-Series Equipment Management System Capacitive Touch Controls on the MFRs rotational electrical magnetic brakes may disengage when an electrocautery device is in use.

## Distribution

Worldwide distribution - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI, WV, and WY. The country of Canada.

## Key facts

- **Recall number:** Z-1297-2021
- **Recalling firm:** Stryker Communications
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-01-29
- **Report date:** 2021-03-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Flower Mound, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1297-2021

## Citation

> AI Analytics. FDA recall Z-1297-2021. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-1297-2021. Source: US FDA. Licensed CC0.

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