Class II — Rymed Technologies, LLC
| Recalling firm | RyMed Technologies, LLC |
|---|---|
| Registered facility | RyMed Technologies, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential for the female luer component of the InVision-Plus IV connector to crack during use. |
| Product | InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use. |
| Quantity | 496,400 units |
| Distribution | US Nationwide Distribution. |
| Initiated | 2016-01-05 |
| Classified | 2016-01-21 |
| Terminated | 2016-10-19 |
| Recall number | Z-0675-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Rymed Technologies, LLC (Z-0675-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/72997/
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