# FDA recall Z-1293-2024

> **Retractable Technologies, Inc.** · Class II · device recall initiated 2024-02-05.

## Product

EasyPoint Needle, 25G x 5/8", REF: 82091

## Reason for recall

The needle cannula of a retractable needle may detach from the needle holder in the patient.

## Distribution

US Nationwide distribution including in the states of NY, FL, IL, MA, UT, NJ, AZ, MO, WA, NC, CA, TX, NV, IN, PA, VA, IA, GA, TN, MI, OH, OK, CO, OR, SC, MN, CT.

## Key facts

- **Recall number:** Z-1293-2024
- **Recalling firm:** Retractable Technologies, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-05
- **Report date:** 2024-03-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Little Elm, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1293-2024

## Citation

> AI Analytics. FDA recall Z-1293-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1293-2024. Source: US FDA. Licensed CC0.

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