FDA Device recall Z-1122-2024
Medline Kits, trays, and packs labeled as follows: a) L&B CDS-LF, REF CDS980273D
- FDA Device
- Class I
- ongoing
- Published 2024-03-06
On 2024-03-06 the FDA classified a Class I recall of Medline Kits, trays, and packs labeled as follows: a) L&B CDS-LF, REF CDS980273D 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-1122-2024 |
| 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, trays, and packs labeled as follows: a) L&B CDS-LF, REF CDS980273D; b) LABOR AND DELIVERY, REF DYNJ907794; c) LACERATION TRAY, REF DYNDL1864A; d) OBSTETRICAL, REF DYNJ908877; e) UMC EP VAGINAL DELIVERY, REF DYNJ83093;
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 CDS980273D, UDI/DI 40884389851808 (case), 10884389851807 (unit), Lot Numbers: 22DBJ834; b) REF DYNJ907794, UD…a) REF CDS980273D, UDI/DI 40884389851808 (case), 10884389851807 (unit), Lot Numbers: 22DBJ834; b) REF DYNJ907794, UDI/DI 40193489884952 (case), 10193489884951 (unit), Lot Numbers: 22BBB085, 22CBW699, 22FBH326, 22KBJ007, 22KBW578, 23ABL612, 23CBT573, 23HBD177; c) REF DYNDL1864A, UDI/DI 40889942721420 (case), 10889942721429 (unit), Lot Numbers: 22FBN858, 22IBN393, 23ABJ223, 23EBK530, 23HBS351; d) REF DYNJ908877, UDI/DI 40195327201747 (case), 10195327201746 (unit), Lot Numbers: 22HBT779, 22KBH144, 22LBM695, 23ABD156; e) REF DYNJ83093, UDI/DI 40195327230870 (case), 10195327230869 (unit), Lot Numbers: 22JME508, 23CMH924, 23DMH299, 23EMC295, 23FMB041 |
|---|
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-1122-2024%22
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