Skip to content

Medline Industries, Inc. DYNJ909951Recalls & reported problems

Medline Industries, Inc. · PLASTIC · Class 1

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

Recalls naming this device

  1. Jun 27, 2024Class IIOpen, Classified

    Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.

    Z-3113-2024 · Root cause: Process control · Recall details · FDA record ↗

Other Plastic surgery and accessories kit devices

All Plastic surgery and accessories kit devices →

Sources and updates

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