# FDA recall Z-0936-2018

> **Medtronic Minimally Invasive Therapies Group** · Class II · device recall initiated 2017-10-24.

## Product

Argyle Suction Tubing (Product # 8888301515)    Argyle  Suction Tubing is an extruded tube used as an extension for different types of devices in an operating room, bonded with 2 female sure grip connectors at each end of the tube to facilitate the plug/ insertion of the device and also includes a male connector that can be used for devices designed with female connectors, This product is sterile, non-conductive and latex free.

## Reason for recall

Incorrect packaging. In one lot of Argyle Suction Tubing, the pouch may be incorrectly labeled as the Salem Sump Dual Lumen Stomach Tube. This product may have been distributed within the case of Argyle Suction Tubing.

## Distribution

USA (nationwide) Distribution

## Key facts

- **Recall number:** Z-0936-2018
- **Recalling firm:** Medtronic Minimally Invasive Therapies Group
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-10-24
- **Report date:** 2018-03-21
- **Termination date:** 2020-10-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0936-2018

## Citation

> AI Analytics. FDA recall Z-0936-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0936-2018. Source: US FDA. Licensed CC0.

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