# FDA recall Z-0490-2018

> **Maquet** · Class II · device recall initiated 2017-05-22.

## Product

Hemofiltration Standard Pack including BC 60 Plus-T 8036.  Part Number: 701066990.    Used in extracorporeal circulation during cardiopulmonary bypass procedures lasting 6 hours or less.

## Reason for recall

55 kits were distributed after their expiration date of September 2015.

## Distribution

Distributed to the states of NM, CA, and IL.

## Key facts

- **Recall number:** Z-0490-2018
- **Recalling firm:** Maquet
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-22
- **Report date:** 2018-02-07
- **Termination date:** 2018-07-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fairfield, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0490-2018

## Citation

> AI Analytics. FDA recall Z-0490-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0490-2018. Source: US FDA. Licensed CC0.

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