# FDA recall Z-1788-2026

> **Cook Incorporated** · Class II · device recall initiated 2026-03-05.

## Product

COOK MEDICAL Spectrum¿ Central Venous Catheter Set:  Reference Part Number C-UDLM-401J-ABRM-HC, Order Number G43983;   Reference Part Number C-UDLM-401J-ABRM-HC-CAH, Order Number G24754;   Reference Part Number C-UDLM-401J-LSC-ABRM-HC, Order Number G43986;   Reference Part Number C-UDLM-401J-PED-ABRM-HC, Order Number G43984;   Reference Part Number C-UDLM-401J-PED-ABRM-HC-CAH, Order Number G24752;   Reference Part Number C-UDLM-401J-RSC-ABRM-HC, Order Number G43985;   Reference Part Number C-UDLM-501J-ABRM-HC, Order Number G43995;   Reference Part Number C-UDLM-501J-PED-ABRM-HC, Order Number G43996;   Reference Part Number C-UDLM-501J-RSC-ABRM-HC, Order Number G43997;   Reference Part Number C-UDLM-801J-ABRM-HC, Order Number G50817;   Reference Part Number C-UQLM-1001J-ABRM-HC-RD, Order Number G51537;   Reference Part Number C-UQLM-1001J-RSC-ABRM-HC-RD, Order Number G51539;   Reference Part Number C-UTLM-501J-ABRM-HC, Order Number G44005;   Reference Part Number C-UTLM-501J-ABRM-HC-CAH

## Reason for recall

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1788-2026
- **Recalling firm:** Cook Incorporated
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-05
- **Report date:** 2026-04-15

- **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-1788-2026

## Citation

> AI Analytics. FDA recall Z-1788-2026. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-1788-2026. Source: US FDA. Licensed CC0.

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