Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1789-2026 — COOK MEDICAL Spectrum¿ Central Venous Tray: Reference Part Number C-UQLMYJ-1001J-RSC-ABRM-HC-FST-A-RD, Order Number G44800; Reference Part Number C-UTLMYJ-701J-ABRM-HC-IHI-FST-A-RD, Order Number G44809; Reference Part Number C-UTLMYJ-701J-RSC-ABRM-HC-FST-A-RD, Order Number G44806; Reference P

U.S. FDA — Device Enforcement · United States · 2026-03-05 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1789-2026
Date of alert: 2026-03-05
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Cook Incorporated
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00827002448001

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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