# FDA recall Z-0634-2018

> **Cook Inc.** · Class II · device recall initiated 2017-07-31.

## Product

Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic Impregnated, Catalog Identifiers: C-UTLMY-501J-ABRM-HC-FST and C-UTLMY-501J-ABRM-HC-IHI-FST    Usage:  The Spectrum Central Venous Catheter is used for the intravenous administration of nutrient fluids, chemotherapeutic agents, and other drugs for therapy, blood sampling, blood delivery, and venous pressure monitoring

## Reason for recall

Central venous catheters may not fit over guide wire potentially causing procedure delay.

## Distribution

Worldwide distribution -  US Nationwide in the states of: AL, CA, CO, FL, GA, IA, IL, KY, LA, MD, MI, MN, MO, NC, NY, OH, OK, OR, PA, RI, TN, TX, UT, VA, WA, WI; the District of Columbia and the countries of  Belgium, India Italy, Spain, and United Kingdom.

## Key facts

- **Recall number:** Z-0634-2018
- **Recalling firm:** Cook Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-31
- **Report date:** 2018-02-21
- **Termination date:** 2019-05-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bloomington, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0634-2018

## Citation

> AI Analytics. FDA recall Z-0634-2018. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0634-2018. Source: US FDA. Licensed CC0.

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