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LSL HEALTHCARE 1555Recalls & reported problems

LSL Industries, LLC · Urine Specimen Collection Kit · 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. Mar 9, 2026Class IIOpen, Classified

    Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.

    Z-1930-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Blood and urine collection kit (excludes HIV testing) devices

All Blood and urine collection kit (excludes HIV testing) devices →

Sources and updates

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