PlainRecalls
FDA Devices Moderate Class II Terminated

JUDKINS PACK

Reported: March 24, 2021 Initiated: February 11, 2021 #Z-1256-2021

Product Description

JUDKINS PACK

Reason for Recall

Component Part Number: 19537LBL (LBL, SHEET OF 39, ASSORTED, STDSZ, MULTI W/BLK INK, WATERPROOF) is being reported as intermittently mixed with an incorrect medication label sheet throughout the specific Presource¿ kit SANHDJTVCF Judkins Pack lot # 525067.

Details

Recalling Firm
Cardinal Health 200, LLC
Units Affected
298 units
Distribution
US state of VA.
Location
Waukegan, IL

Frequently Asked Questions

What product was recalled?
JUDKINS PACK. Recalled by Cardinal Health 200, LLC. Units affected: 298 units.
Why was this product recalled?
Component Part Number: 19537LBL (LBL, SHEET OF 39, ASSORTED, STDSZ, MULTI W/BLK INK, WATERPROOF) is being reported as intermittently mixed with an incorrect medication label sheet throughout the specific Presource¿ kit SANHDJTVCF Judkins Pack lot # 525067.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 24, 2021. Severity: Moderate. Recall number: Z-1256-2021.