# FDA recall Z-2827-2017

> **International Medsurg Connection, Inc.** · Class II · device recall initiated 2017-06-23.

## Product

Piston Syringe and Hypodermic Needle, 1 CC TB 28 G X 0.5, 100 per box, 30 boxes/case, 3,000/case

## Reason for recall

Insufficient documentation to support product sterility claims.

## Distribution

Nationwide Distribution including OH, MA, GA, FL, NC, MS, MO, PA, IN, NJ, TX, KS, LA, NE, WA, AL, UT, AK, CA, IL, MN, MD, NY, and MI.

## Key facts

- **Recall number:** Z-2827-2017
- **Recalling firm:** International Medsurg Connection, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-23
- **Report date:** 2017-08-16
- **Termination date:** 2020-08-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Schaumburg, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2827-2017

## Citation

> AI Analytics. FDA recall Z-2827-2017. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-2827-2017. Source: US FDA. Licensed CC0.

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