FDA Device recall Z-1092-2024
MEDLINE kits and trays, labeled as: a) SUCTION CATH 10FR KIT W/SALINE, REF DYND41470SA, DYND41470SAH
- FDA Device
- Class I
- ongoing
- Published 2024-03-06
On 2024-03-06 the FDA classified a Class I recall of MEDLINE kits and trays, labeled as: a) SUCTION CATH 10FR KIT W/SALINE, REF DYND41470SA, DYND41470SAH by Medline Industries Northfield, citing medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1092-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-11-15 |
| Published | 2024-03-06 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
MEDLINE kits and trays, labeled as: a) SUCTION CATH 10FR KIT W/SALINE, REF DYND41470SA, DYND41470SAH; b) TRACH CARE TRAY, REF DYNDA1931B, DYNDA1931BH
Reason
Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride Irrigation USP, Sterile Water for Irrigation USP and Saline Flush Syringe. Nurse Assist issued a recall due to the potential lack of sterility, which could result in the solution being non sterile.
Identifiers
| code_info | a) REF DYND41470SA, UDI/DI 40884389338705 (case), 10884389338704 (unit), Lot Numbers: 22HBD360, 22IBA256, 23ABU349, 23…a) REF DYND41470SA, UDI/DI 40884389338705 (case), 10884389338704 (unit), Lot Numbers: 22HBD360, 22IBA256, 23ABU349, 23CBG160, 23GBV051, 23IBT355; REF DYND41470SAH; UDI/DI - same as DYND41470SA, Lot Numbers: 22HBD360, 22IBA256, 23ABU349, 23CBG160, 23GBV051, 23IBT355; b) REF DYNDA1931B, UDI/DI 40195327277360 (case), 10195327277369 (unit), Lot Numbers: 22LMC118, 22LMC126, 23EMB086; REF DYNDA1931BH, UDI/DI - same as DYNDA1931B, Lot Numbers: 22LMC118, 22LMC126, 23EMB086 |
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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-1092-2024%22
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