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.
Take action
Contact the company
📍Recalling firmCardinal Health 200, LLC3651 Birchwood Dr · Waukegan, IL 60085-8337
“Cardinal Health Judkins Pack Recall: Incorrect Medication Label Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63278-cardinal-health-judkins-pack-recall-incorrect-medication-label-risk. Based on FDA recall #Z-1256-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1256-2021%22&limit=1).
Cardinal Health 200, LLC voluntarily recalled JUDKINS PACK model SANHDJTVCF, lot 525067, due to intermittent mixing with incorrect medication label sheets, the FDA said on Feb. 11, 2021. The recall affects 298 units distributed in Virginia.
How to tell if you have it
Brand: Cardinal Health
Product: JUDKINS PACK
Model: SANHDJTVCF
Lot: 525067
The hazard
Component Part Number 19537LBL is being reported as intermittently mixed with an incorrect medication label sheet throughout the specific Presource kit SANHDJTVCF Judkins Pack lot 525067, according to FDA records.
Context
GovInfoNow's records show Cardinal Health 200, LLC has 59 other recalls on record since June 27, 2017. Other recent recalls of similar products include Presource Packs with Microstream Components Risk of Delayed Treatment (Aug. 19, 2026), Presource Gyn Laparoscopy Kits May Leak Fluids During Use - Recall (Aug. 18, 2026), and Cardinal Health 200, LLC recalls Presource Convenience Kits (Aug. 10, 2026). Medline convenience kits were recalled for potential contamination on July 10, 2026.
How to tell if you have this one
Check for the Judkins Pack model SANHDJTVCF with lot number 525067. The product was sold by Cardinal Health 200, LLC.
Brand
Cardinal Health
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Stop Using Immediately
Discard the Judkins Pack model SANHDJTVCF lot 525067 if you have it.
Where it went and when
Where it was distributed
Distributed in Virginia.
Listed by the agency
Not listed
FDA distribution: “US state of VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Virginia.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1256-2021 (February 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1256-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.