# FDA recall Z-1114-2026

> **SunMed Holdings, LLC** · Class I · device recall initiated 2025-12-15.

## Product

Brand Name: Broselow  Product Name: Broselow Pediatric Emergency Rainbow Tape  Model/Catalog Number: 7700REA  Software Version: Not Applicable  Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.  Component: No

## Reason for recall

Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Hong Kong, and Singapore.

## Key facts

- **Recall number:** Z-1114-2026
- **Recalling firm:** SunMed Holdings, LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-15
- **Report date:** 2026-02-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Grand Rapids, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1114-2026

## Citation

> AI Analytics. FDA recall Z-1114-2026. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1114-2026. Source: US FDA. Licensed CC0.

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