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SAFE-T-FILL® 07 6013Recalls & reported problems

Ram Scientific, Inc · SAFE-T-FILL® Micro Capillary Blood Collection, 125 µL; Prepared with Dipotassium EDTA; Self-sealing Cap, Purple · Class 2

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. May 5, 2025Open, 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 · FDA record ↗

Other Tubes, vials, systems, serum separators, blood collection devices

All Tubes, vials, systems, serum separators, blood collection devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.