FDA Device recall Z-0676-2016
InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001
- FDA Device
- Class II
- terminated
- Published 2016-01-27
On 2016-01-27 the FDA classified a Class II recall of InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001 by Rymed Technologies, citing potential for the female luer component of the InVision-Plus IV connector to crack during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0676-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-01-05 |
| Published | 2016-01-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Rymed Technologies |
| Distribution | US |
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
Potential for the female luer component of the InVision-Plus IV connector to crack during use.
Identifiers
| code_info | Catalog number RYM-7001 Lots: R01842, R01889, R01891, and R01897, Expire 03/2016. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0676-2016%22
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