# FDA recall Z-2811-2017

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

## Product

Hypodermic Needle, 20 G X 1.5 in BD YALE DISP RG, 100 per box, 50 boxes/case, 5,000/case    The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatment or prevention of disease, or to affect the structure or any function of the body.

## 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-2811-2017
- **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-2811-2017

## Citation

> AI Analytics. FDA recall Z-2811-2017. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/Z-2811-2017. Source: US FDA. Licensed CC0.

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