# FDA recall Z-2243-2020

> **Med Tec Inc** · Class II · device recall initiated 2020-05-12.

## Product

Type S Extension For use with Varian, CIVCO, Prescription Only - Product Usage: Device is intended for patient positioning.

## Reason for recall

Potential for disengagement of the Varian Style Type-S Extension during patient repositioning.  The risk associated with the disengagement of the extension could be a patient fall if the patient is not supported by clinical staff.

## Distribution

Worldwide distribution - US Nationwide distribution including in the states of WI, TX, AZ, FL, NE, TN, MA, FL, GA, IN, OR, PA, IL, LA, NH, MS, MI, OH, MN, VA, IA, CA, NC, SC, AK, UT, WA, MO, MT, KS, and WV.    The countries of Africa, Colombia, Saudi Arabia, Costa Rica, South Korea, Hungary, Spain, and Italy.

## Key facts

- **Recall number:** Z-2243-2020
- **Recalling firm:** Med Tec Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-05-12
- **Report date:** 2020-06-10
- **Termination date:** 2021-03-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Orange City, IA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2243-2020

## Citation

> AI Analytics. FDA recall Z-2243-2020. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2243-2020. Source: US FDA. Licensed CC0.

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