Z-1256-2021 Class II Terminated
FDA device recall Z-1256-2021 was initiated by Cardinal Health 200, LLC on February 11, 2021 and is designated Class II. 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 speci… The recall status is terminated (terminated December 22, 2022). Affected quantity: 298 units.
Recall Details
- Product Type
- Devices
- Report Date
- March 24, 2021
- Initiation Date
- February 11, 2021
- Termination Date
- December 22, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 298 units
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.
Distribution Pattern
US state of VA.
Code Information
Model SANHDJTVCF, lot 525067.