# FDA recall Z-1438-2023

> **ROi CPS LLC** · Class II · device recall initiated 2023-03-22.

## Product

Sterile surgical convenience kits:    1.  regard Item Number:  880473001, OR01105A - Total Shoulder/Hip; 2.  regard Item Number:  880426004, OR01033D - Total Hip; 3.  regard Item Number:  880427003, OR01034C - Total Knee; 4.  regard Item Number:  880474001, OR01106A - Knee Arthroscopy; 5.  regard Item Number:  800772006, OR00977F - OH Total Knee Pack ; 6.  regard Item Number:  880403004, OR01009D - Extremity Pack; 7.  regard Item Number:  880472001, OR01104A - Basic Pack ; 8.  regard Item Number:  880470001, OR01102A - Total Knee ; 9.  regard Item Number:  800755006, OR00960F - OH Hip Pack ; 10.  regard Item Number:  880471001, OR01103A - Shoulder Arthroscopy ; 11.  regard Item Number:  880480001, OR01112A - Hand and Foot ; and 12.  regard Item Number:  880468001, OR01100A - Spine.

## Reason for recall

The recalling firm was notified by their supplier that the light handle covers may separate from the light handle and fall off during use.  The light handle covers are a kit component.

## Distribution

US Nationwide distribution in the states of FL and MO.  There was no foreign/military/government distribution.

## Key facts

- **Recall number:** Z-1438-2023
- **Recalling firm:** ROi CPS LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-22
- **Report date:** 2023-05-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Republic, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1438-2023

## Citation

> AI Analytics. FDA recall Z-1438-2023. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1438-2023. Source: US FDA. Licensed CC0.

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