FDA recall record

Medtronic HR-ACT recall — FDA Z-0539-2026

Medtronic personnel observed trace amounts of dry blood on the external carton label and Instructions for Use (IFU) in five boxes of one lot of ACT…

Class IIclassification
Z-0539-2026official record ID
Nov 26, 2025report date

Recall record at a glance

Official recordZ-0539-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMedtronic Perfusion Systems
Report dateNov 26, 2025
Recall initiation dateOct 20, 2025
Quantity3850 units
LocationBrooklyn Park, MN, United States

Official product description

Medtronic HR-ACT (High Range Activated Clotting Time Cartridges), REF 402-03

Why the product was recalled

Medtronic personnel observed trace amounts of dry blood on the external carton label and Instructions for Use (IFU) in five boxes of one lot of ACT Cartridges.

Distribution information

US Nationwide distribution in the states of Hawaii and New York.

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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