# FDA recall Z-2759-2017

> **Smiths Medical ASD Inc.** · Class II · device recall initiated 2016-12-09.

## Product

Smiths Medical CADD Blue-Striped IV Administration Set, REF 21-7036-01, Sterilized using ethylene oxide.

## Reason for recall

The label of the CADD Blue-Striped Administrative Set is missing the expiration date, which is considered a regulatory compliance issue for Canada.

## Distribution

Canada only

## Key facts

- **Recall number:** Z-2759-2017
- **Recalling firm:** Smiths Medical ASD Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2016-12-09
- **Report date:** 2017-08-02
- **Termination date:** 2017-12-14

- **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-2759-2017

## Citation

> AI Analytics. FDA recall Z-2759-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2759-2017. Source: US FDA. Licensed CC0.

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