# FDA recall Z-3083-2017

> **Med Tec Inc** · Class II · device recall initiated 2017-08-10.

## Product

CIVCO Arm Support, REF 106047, distributed as:  (a) Rigid Arm Support, Large, Set, Red (PN: 106047)  (b) PB2-BDLRL (PN: 109040)  (c) Rigid Adj. Arm Support, Large, Set (PN: 106048)  (d) PSR2-CF-DLRL-2P Posirest-2 (PN: 106522)    The Rigid Arm Supports are utilized on the Posibboard2 and Posirest assemblies, which are intended to position the patients upper extremities during breast and lung diagnostic and radiotherapy treatment.

## Reason for recall

Rigid Arm Supports (PN:  106015 and 106047), which were used as part of the Posiboard-2 and Posirest, and were distributed as PN: 106015, 106047, 106521, 106522, 109030, and 109040 between Ocotober 2009 and July 2012 may have a height difference of approximately 17mm.

## Distribution

Worldwide Distribution - US Distribution to the states of : MI, IL and TX.,  and to the countries of : Greece, Australia, Czech Republic, Hungary, Norway, Brazil, Italy, Switzerland ,UK, Austria, Slovenia, Croatia,  Poland, Germany, Japan, France, Netherland, Sri Lanka, Pakistan, Bangladesh, and Israel

## Key facts

- **Recall number:** Z-3083-2017
- **Recalling firm:** Med Tec Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-08-10
- **Report date:** 2017-09-06
- **Termination date:** 2024-03-19

- **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-3083-2017

## Citation

> AI Analytics. FDA recall Z-3083-2017. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-3083-2017. Source: US FDA. Licensed CC0.

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