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MEDLINE DYK1000TSERecalls & reported problems

Medline Industries, Inc. · TUBULAR SPONGE, ENZYMATIC · 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. Apr 21, 2022Class IIOpen, Classified

    Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.

    Z-1217-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other ACCESSORIES, CLEANING BRUSHES, FOR ENDOSCOPE devices

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Sources and updates

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