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SOL-M Luer Lock Syringe w/Exch NeedleRecalls & reported problems across all models

Sol-Millennium Medical, Inc. · 2 models in the FDA device registry

Data updated Oct 18, 2026 from official FDA records · Editorial policy

1 open recall names at least one SOL-M Luer Lock Syringe w/Exch Needle model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls
1

We found 2 models of SOL-M Luer Lock Syringe w/Exch Needle by Sol-Millennium Medical, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

SOL-M Luer Lock Syringe w/Exch Needle recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. May 9, 2024Class IIOpen, Classified

    Products in distribution were found by FDA to be to be substantially different from the current cleared 510(k)s with a major change or modification to the device s intended use.

    Z-3075-2024 · Root cause: Other · names 2 of these models · Recall details · FDA record ↗

SOL-M Luer Lock Syringe w/Exch Needle models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

Other Sol-Millennium Medical, Inc. products

All Sol-Millennium Medical, Inc. devices →

Sources and updates

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