Arrow Kits with Medtronic Covidien 0 — Class II medical device recall Z-2825-2015
Terminated recall by Arrow International Inc, reported 2015-10-07, distributed nationwide. Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to compromised sterility of the outer barrel,
| Recall number | Z-2825-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arrow International Inc, Reading, PA, United States |
| Recall initiated | 2015-08-27 |
| Classified | 2015-09-30 |
| Reported by FDA | 2015-10-07 |
| Terminated | 2018-06-18 |
| Distributed | Nationwide (US) |
| Quantity | 73,714 |
| Reason classes | sterility |
| Lot numbers | 23F15C0042, 23F15C0239, 23F15C0348, 23F15C0685, 23F15C0708, 23F15C0997, 23F15C1111, 23F15C1116, 23F15C1146, 23F15C1225, 23F15C1226, 23F15C1232, 23F15C1318, 23F15C1321, 23F15C1509, 23F15C1552, 23F15C1553, 23F15C1687, 23F15C1705, 23F15C1719, 23F15C1828, 23F15C1832, 23F15C1839, 23F15C1840, 23F15C1842, 23F15C1843, 23F15C1845, 23F15C1848, 23F15C1850, 23F15C1896, 23F15C1898, 23F15C1909, 23F15C1911, 23F15C1964, 23F15C1969, 23F15C1972, 23F15C1974, 23F15C2121, 23F15C2257, 23F15C2259 and 265 more |
Product
Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes
Reason for recall
Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to compromised sterility of the outer barrel, Arrow purchased recalled items that were packaged with certain 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-2825-2015. 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.