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MAXORB EXTRA AlginateRecalls & reported problems

Medline Industries, Inc. · 14-21BP · Class 1

Data updated Oct 13, 2026 from official FDA records · Editorial policy

1 open recall names 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
1

Summary

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

1 FDA recall record name this device's identifier, 1 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Oct 1, 2024Open, Classified

    Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.

    Z-0619-2025 · Root cause: Packaging process control · FDA record ↗

Other Dressing, Wound, Hydrophilic devices

All Dressing, Wound, Hydrophilic devices →

Sources and updates

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