Cook Incorporated: Device Recall

Recall Details

Recall Number

Z-2223-2024

Classification

Class II

Product Type

Device

Recalling Firm

Cook Incorporated

Status

Ongoing

Date Initiated

05/15/2024

Location

Bloomington, IN, United States

Voluntary/Mandated

Voluntary: Firm initiated

Product Quantity

15 units

Reason for Recall

Product labels state the incorrect expiration dates that extends beyond their true expiration date

Product Description

Ultrathane Cook-Cope Type Locking Loop Multipurpose Drainage Catheter-ULT12.0-38-45-P-6S-CLM-RH-ntended for percutaneous drainage in a variety of drainage applications (e.g., nephrostomy, biliary and abscess), either by direct stick or Seldinger access technique ORDER NUMBER: GPN:G09767

Distribution Pattern

MA Foreign: Spain, and Netherlands

Other Recalls by Cook Incorporated

• Class II: Risk 11/26/2025
  Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.
• Class II: Risk 11/26/2025
  Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.
• Class II: Risk 11/26/2025
  Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.
• Class I: Dangerous 05/15/2025
  Cook Medical identified that catheters supplied in the affected device lots may experience tip separation.
• Class II: Risk 04/17/2025
  Cook Medical identified that devices from the affected device lots may contain the incorrectly sized introducer sheath.

View all recalls by Cook Incorporated →