# FDA recall Z-1252-2021

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2021-02-09.

## Product

Magellan 3 mL Syringe with Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin.      Product Code: 8881833558

## Reason for recall

Safety shield not locking into the cannula. If the safety shield activation fails to lock a contaminated needle, a needlestick may occur and there is the potential for exposure to bloodborne pathogens

## Distribution

Worldwide distribution - US Nationwide distribution and the countries of AE, Japan.

## Key facts

- **Recall number:** Z-1252-2021
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-02-09
- **Report date:** 2021-03-24
- **Termination date:** 2024-04-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1252-2021

## Citation

> AI Analytics. FDA recall Z-1252-2021. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1252-2021. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*