# FDA recall Z-2662-2018

> **Smiths Medical ASD Inc.** · Class II · device recall initiated 2018-04-13.

## Product

Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism

## Reason for recall

Certain Barrel Clamp Guides may contain a ridge that could potentially lead to spring slippage, resulting in the inability of the pump to recognize a loaded syringe or the pump, misidentifying the size of a loaded syringe.

## Distribution

US distribution to AL, AZ, CA, DC, FL, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NJ, NM, NY, OH, OK, PA, TN, TX, UT, VA, WA.      International distribution to Canada and Lebanon.

## Key facts

- **Recall number:** Z-2662-2018
- **Recalling firm:** Smiths Medical ASD Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-04-13
- **Report date:** 2018-08-15
- **Termination date:** 2023-01-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Minneapolis, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2662-2018

## Citation

> AI Analytics. FDA recall Z-2662-2018. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-2662-2018. Source: US FDA. Licensed CC0.

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