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SAFE-T-FILL® 07 7058Recalls & reported problems

Ram Scientific, Inc · SAFE-T-FILL® Micro Capillary Blood Collection, 200 µL; Prepared with Dipotassium EDTA; Flat Bottom Microtube, Purple · Class 2

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. May 5, 2025Class IIOpen, Classified

    All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured between July 31, 2023 to February 28, 2025 cause false positive results when used with Magellan Diagnostics LeadCare Testing Systems. False positive lead results may cause delayed results and additional unnecessary testing.

    Z-0372-2026 · Root cause: Component design/selection · Recall details · FDA record ↗

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Sources and updates

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