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Medline Industries, Inc. DYNDH1561Recalls & reported problems

Medline Industries, Inc. · PERIPHERAL BLOOD CULTURE DRAW · 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. Nov 1, 2023Class IIOpen, Classified

    This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.

    Z-0311-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  2. Sep 9, 2022Class IIOpen, Classified

    Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.

    Z-0121-2023 · Root cause: Process control · Recall details · FDA record ↗

Other Wound dressing kit devices

All Wound dressing kit devices →

Sources and updates

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