FDA Device recall Z-2825-2015
Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes
- FDA Device
- Class II
- terminated
- Published 2015-10-07
On 2015-10-07 the FDA classified a Class II recall of Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes by Arrow International, citing 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 produ….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2825-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-27 |
| Published | 2015-10-07 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Arrow International |
| Distribution | US |
Product
Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes
Reason
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.
Identifiers
| code_info | ASK-01000-CK ASK-01552-DMI ASK-02041-JHVA1 ASK-04000-WA ASK-04000-WA ASK-04001-CG1 ASK-04001-CG1 ASK-04001-DU4S…ASK-01000-CK ASK-01552-DMI ASK-02041-JHVA1 ASK-04000-WA ASK-04000-WA ASK-04001-CG1 ASK-04001-CG1 ASK-04001-DU4S ASK-04001-DU5S ASK-04001-DU5S ASK-04001-DU7 ASK-04001-DU8 ASK-04001-DU8 ASK-04001-MC ASK-04001-MC ASK-04001-UOC ASK-04001-VCUH ASK-04001-VCUH ASK-04001-VCUH ASK-04001-VCUH ASK-04020-BH ASK-04301-HH1 ASK-04500-BGH ASK-04510-MM3 ASK-04510-MM3 ASK-05052-QV ASK-05052-QV ASK-05052-SFL ASK-05502-UWMC ASK-05502-UWMC ASK-05502-UWMC ASK-09600-FAM ASK-09804-SPH ASK-09804-SPH ASK-09810-PCMH1 ASK-09903-ECL ASK-45703-PUHS ASK-45703-PUIC ASK-45703-PUIC ASK-45703-PUR1 ASK-45703-PUW1 ASK-45703-PUW1 ASK-45703-PVAL ASK-45703-PVCU ASK-45703-PVCU ASK-45703-PVCU ASK-45703-SHB1 ASK-45703-SJM ASK-45703-SJM ASK-45703-UHC ASK-45703-WA ASK-45703-WA ASK-45802-PCMH1 ASK-45854-NG ASK-45854-NG ASK-45854-PCCH1 ASK-45854-PCCH1 ASK-45854-PCHS1 ASK-45854-PCHS1 ASK-45854-PDCH1 ASK-45854-PFAM ASK-45854-PLGH ASK-45854-PNM ASK-45854-PNM ASK-45854-PPC |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2825-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.