Mini Stick MAX H965457490Recalls & reported problems
Angiodynamics, Inc. · Mini Stick MAX Coaxial Microintroducer Kit · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 15051684022927), received between Aug 7, 2025 and Aug 7, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
14 other recalls cover devices cleared under the same FDA submission (K132713); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Recalls naming this device
- Jan 30, 2024Open, Classified
Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case
Z-1334-2024 · Root cause: Process control · FDA record ↗
Most reported problems
Device problems
- Material Split, Cut or Torn1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 7, 2025Material Split, Cut or Torn
USED MINISTICK MAX FOR ACCESS TO RIGHT FEMORAL ARTERY. MOST OF EXTERIOR CATHETER SPLIT INTO PATIENT. HAD TO CALL DR [(B)(6)] TO CUT DOWN AND REMOVE DEVICE. PATIENT INTUBATED AND SENT TO ICU.
Patient problems: Foreign Body In Patient
MAUDE report 22737194 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K132713. One submission often covers many models, so check the product and lot details in each record.
- Z-1348-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. - Catalog Number: 45-781
- Z-1339-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756
- Z-1344-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767
- Z-1337-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 4F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-752
- Z-1347-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 5F X 15 CM STIFF .018 NI/TU NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-776
- Z-1336-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-751
- Z-1342-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 4F X 10 CM STIFF .018 NI/TU NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-762
- Z-1340-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 5F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-758
- Z-1345-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-774
- Z-1343-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-765
- Z-1341-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759
- Z-1335-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750
- Z-1346-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-775
- Z-1338-2024 · Jan 30, 2024 · Open, ClassifiedMINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-754
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- AVANTI 504656XCordis Corporation · DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION1 recall2 reports
- Mini Stick MAX H965457510Angiodynamics, Inc. · DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION1 recall1 report
- Abiomed® 00884450732311Merit Medical Systems, Inc. · Dilator, Vessel, For Percutaneous Catheterization1 recall1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.