InVision-Plus CS Needleless IV Connector — Class II medical device recall Z-0676-2016
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-0676-2016 |
|---|---|
| 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 | 46,600 units |
| Reason classes | packaging |
| Lot numbers | R01842, R01889, R01891, R01897 |
| Model numbers | R01842, R01889, R01891, R01897, RYM-7001 |
Product
InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. 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-0676-2016. 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.