FDA Device recall Z-2526-2025
Smiths Medical CADD Medication Cassette Reservoir with flow stop, clamp and female Luer
- FDA Device
- Class II
- ongoing
- Published 2025-09-10
On 2025-09-10 the FDA classified a Class II recall of Smiths Medical CADD Medication Cassette Reservoir with flow stop, clamp and female Luer by Icu Medical, citing certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in med….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2526-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-08-06 |
| Published | 2025-09-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Icu Medical |
| Distribution | n/a |
Product
Smiths Medical CADD Medication Cassette Reservoir with flow stop, clamp and female Luer. Non-vented stopper included. 100mL, Product Code 21-7302-24
Reason
Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.
Identifiers
| code_info | UDI/DI 10610586027239, Lot Numbers: 4468669, 4468670, 4468671, 4468677, 6004936, 6005591, 6005593, 6005601, 6012443, 60…UDI/DI 10610586027239, Lot Numbers: 4468669, 4468670, 4468671, 4468677, 6004936, 6005591, 6005593, 6005601, 6012443, 6012470, 6012472, 6012474, 6012477, 6022033, 6022034, 6022039, 6022040, 6022041, 6022045, 6022046, 6022047, 6022048, 6022049, 6022051, 6022053, 6026851, 6026853, 6026854, 6026855, 6026856, 6026857, 6026858, 6026859, 6026861, 6026862, 6026863, 6026864, 6026865, 6026866, 6026867, 6026868, 6026869, 6026870, 6026872, 6026873, 6026874, 6026875, 6037772, 6037773, 6037774, 6037775, 6037776, 6037777, 6037778, 6037779, 6037780, 6037781, 6037782, 6053814, 6054005, 6054007, 6054008, 6054009, 6054010, 6054011, 6054013, 6054014, 6056238, 6062718, 6054012, 6062712, 6062710, 6062699, 6062714, 6062700, 6062701, 6062702, 6062705, 6062716, 6062703, 6062706, 6062721, 6062711, 6062723, 6062717 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2526-2025%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.