InVision-Plus and InVision-Plus Junior Needleless IV Connector — Class II medical device recall Z-0675-2016
Terminated recall by Rymed Technologies, LLC, reported 2016-01-27, distributed nationwide. Potential for the female luer component of the InVision-Plus IV connector to crack during use.
| Recall number | Z-0675-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Rymed Technologies, LLC, Austin, TX, United States |
| Recall initiated | 2016-01-05 |
| Classified | 2016-01-21 |
| Reported by FDA | 2016-01-27 |
| Terminated | 2016-10-19 |
| Distributed | Nationwide (US) |
| Quantity | 496,400 units |
| Reason classes | packaging |
| Lot numbers | 610, 611, 613, 614, R01777, R01789, R01807, R01817, R01822, R01825, R01827, R01839, R01848, R01853, R01857, R01860, R01871, R01874, R01887, R01890 |
| Model numbers | 610, 611, 613, 614, R01777, R01789, R01807, R01817, R01822, R01825, R01827, R01839, R01848, R01857, R01860, R01871, R01874, R01887, R01890, RYM-5000, RYM-5001, RYM-5001CL, RYM-8001 |
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.
Reason for recall
Potential for the female luer component of the InVision-Plus IV connector to crack during use.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0675-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.