Convenience Kits from Centurion that contain an In-Vision- Plus… — Class II medical device recall Z-0861-2016
Terminated recall by Centurion Medical Products Corporation, reported 2016-03-02, distributed in CA, FL, GA, IL, PA, TN, TX, VA. Convenience Kits contain an In-Vision-Plus Needleless IV Connector, code RYM5001 that is being recalled by the
| Recall number | Z-0861-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Centurion Medical Products Corporation, Williamston, MI, United States |
| Recall initiated | 2016-01-19 |
| Classified | 2016-02-23 |
| Reported by FDA | 2016-03-02 |
| Terminated | 2016-07-19 |
| Distributed | CA, FL, GA, IL, PA, TN, TX, VA |
| Quantity | 1,130 |
| Reason classes | packaging, device malfunction |
| Lot numbers | 16CM, 2015040850, 2015041350, 2015041450, 2015041550, 2015041750, 2015042150, 2015042750, 2015052150, 2015052250, 2015052750, 2015060150, 2015060450, 2015061050, 2015061150, 2015061550, 2015061850, 2015062250, 2015062650, 2015070150, 2015070250, 2015070950, 2015071050, 2015071750, 2015080550, 2015080650, 2015080750, 2015081150, 2015081350, 20CM, 3XICVC, 6FR, ECVC1025, ECVC1425, ECVC1780, ECVC1785, ECVC3015CVC, ECVC3260CVC, ECVC3540, ECVC3575CVC and 7 more |
| Model numbers | RYM5001 |
Product
Convenience Kits from Centurion that contain an In-Vision- Plus Needleless IV Connector, Model: code RYM5001 InVision-Plus¿ Needless IV Connectors are used for single patient use in IV and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.
Reason for recall
Convenience Kits contain an In-Vision-Plus Needleless IV Connector, code RYM5001 that is being recalled by the manufacturer, RyMed Technologies, LLC. A component molding abnormality may cause female luer threads to crack, leading to potential for the mating tubing set to become detached and for the administration to be interrupted. Other components within these kits are not affected.
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-0861-2016. 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.