FDA recall record

Cardinal Health 200 JUDKINS PACK recall — FDA Z-1256-2021

Component Part Number: 19537LBL (LBL, SHEET OF 39, ASSORTED, STDSZ, MULTI W/BLK INK, WATERPROOF) is being reported as intermittently mixed with an…

Class IIclassification
Z-1256-2021official record ID
Mar 24, 2021report date

Recall record at a glance

Official recordZ-1256-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCardinal Health 200, LLC
Report dateMar 24, 2021
Recall initiation dateFeb 11, 2021
Quantity298 units
LocationWaukegan, IL, United States

Official product description

JUDKINS PACK

Why the product was 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.

Distribution information

US state of VA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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