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Medline Industries, Inc. DYNJ36725BRecalls & reported problems

Medline Industries, Inc. · VENOUS ACCESS PACK-LF · Class 2

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

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.

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. Oct 27, 2021Class IITerminated

    NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after 04/2020.

    Z-0361-2022 · Root cause: Incorrect or no expiration date · Recall details · FDA record ↗

Other Central venous catheter tray devices

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Sources and updates

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