# FDA recall Z-3071-2017

> **Smiths Medical ASD Inc.** · Class II · device recall initiated 2017-06-05.

## Product

CADD(R) Medication Cassette Reservoir with clamp and female Luer.  Non vented stopper included, REF 21-7002-24, Rx only, STERILE EO, Manufacturer Smiths Medical ASD, Inc.

## Reason for recall

The medication cassette reservoir, part number  21-7002-24, with lot number 16X659, may have been manufactured with the incorrect pressure plate and the tubing used on the cassette may have been routed  incorrectly.

## Distribution

Japan, China, US

## Key facts

- **Recall number:** Z-3071-2017
- **Recalling firm:** Smiths Medical ASD Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-05
- **Report date:** 2017-09-06
- **Termination date:** 2020-08-04

- **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-3071-2017

## Citation

> AI Analytics. FDA recall Z-3071-2017. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-3071-2017. Source: US FDA. Licensed CC0.

---

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