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Medline Industries, Inc. DYNJ61383CRecalls & reported problems

Medline Industries, Inc. · PERIPHERAL ARTERIOGRAM RAD · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. Feb 27, 2026Class IIOpen, Classified

    Unapproved design changes to the products outside of the 510(k) clearance.

    Z-1890-2026 · Root cause: Component change control · Recall details · FDA record ↗

  2. Feb 27, 2026Class IIOpen, Classified

    Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.

    Z-2590-2026 · Root cause: No Marketing Application · Recall details · FDA record ↗

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page