Z-1051-2024 Class I Ongoing

Recalled by Cardinal Health 200, LLC — Waukegan, IL

FDA device recall Z-1051-2024 was initiated by Cardinal Health 200, LLC on December 4, 2023 and is designated Class I. Reason for recall: Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist. The recall status is ongoing. Affected quantity: 36300 units.

Recall Details

Product Type
Devices
Report Date
February 28, 2024
Initiation Date
December 4, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
36300 units

Product Description

Dover" 100% SILICONE 400ML U/M TEMP SENSE FOLEY TRAY, LL, 18 FR (6.0 MM), 5CC, 2000ML DRAIN BAG, CSD

Reason for Recall

Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.

Distribution Pattern

US and EMEA, Japan, Latin America

Code Information

7946, UDI/DI 20884521029559 (cs), 10884521029552 (ea), Lot Numbers: 2222832064, 2301031864, 2317001864, 2209526164, 2215827064, 2317731864, 2305204964, 2305205064, 2210226764, 2208817764