# FDA recall Z-0315-2018

> **Centurion Medical Products Corporation** · Class II · device recall initiated 2017-07-05.

## Product

SafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in  Centurion Convenience Kits.   Centurion component code BD17O1NS.

## Reason for recall

Centurion is recalling specific  lots of convenience kits, SafetyGlide Needle, 22GA 1-1/2in, manufactured by BD, sold in  Centurion Convenience Kits. distributed between May 2016 and June 2017 due to notice received from BD's recall due to particulate that could be expelled out of the needle if used for injection.

## Distribution

US.

## Key facts

- **Recall number:** Z-0315-2018
- **Recalling firm:** Centurion Medical Products Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-05
- **Report date:** 2018-01-10
- **Termination date:** 2018-03-09

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0315-2018

## Citation

> AI Analytics. FDA recall Z-0315-2018. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0315-2018. Source: US FDA. Licensed CC0.

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