FDA Device recall Z-1256-2021
JUDKINS PACK
- FDA Device
- Class II
- terminated
- Published 2021-03-24
On 2021-03-24 the FDA classified a Class II recall of JUDKINS PACK by Cardinal Health 200, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1256-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-02-11 |
| Published | 2021-03-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Cardinal Health 200 |
| Distribution | VA |
Product
JUDKINS PACK
Reason
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.
Identifiers
| code_info | Model SANHDJTVCF, lot 525067. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1256-2021%22
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