Catheter — Class II medical device recall Z-2774-2016
Terminated recall by Arrow International Inc, reported 2016-09-21, distributed in FL, MD, NC, OH. Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) produ
| Recall number | Z-2774-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2016-02-17 |
| Classified | 2016-09-09 |
| Reported by FDA | 2016-09-21 |
| Terminated | 2017-10-18 |
| Distributed | FL, MD, NC, OH |
| Quantity | 6,121 units |
| Lot numbers | 23F15C1225, 23F15C1226, 23F15D0241, 23F15D1514, 23F15E1091, 23F15E1094, 23F15F0358, 23F15F1836, 23F15G0159, 23F15G0871, 23F15H0014, 23F15H0020, 23F15H0740, 23F15H0857, 23F15H0919, 23F15H1033, 23F15J0259, 23F15J0260, 23F15J0285, 23F15J0431, 23F15J0533, 23F15J1102, 23F15K0012, 23F15K0345, 23F15K0983, 23F15K1009, 23F15L0662, 23F15M0313, 23S15G0973 |
Product
Catheter, Intravascular, Therapeutic, Short-Term Less than 30 days The Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access.
Reason for recall
Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.
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-2774-2016. 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.