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Medline Industries, Inc. DYNJ0248546DRecalls & reported problems

Medline Industries, Inc. · MAXIMUM BARRIER PACK-LF · 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. May 18, 2023Class IIOpen, Classified

    Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.

    Z-2179-2023 · Root cause: Device Design · Recall details · FDA record ↗

  2. Dec 27, 2022Class IIOpen, Classified

    The convenience trays had improper placement of some of the components that were in the nonsterile portion of the tray, thus, not receiving sterilization.

    Z-1162-2023 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

Other General surgery tray devices

All General surgery tray devices →

Sources and updates

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