Z-1109-2024 Class I Ongoing

Recalled by MEDLINE INDUSTRIES, LP - Northfield — Northfield, IL

FDA device recall Z-1109-2024 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Nov 15, 2023 and is designated Class I. Reason for recall: 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… The recall status is ongoing. Affected quantity: 139 units.

Recall Details

Product Type
Devices
Report Date
Mar 6, 2024
Initiation Date
Nov 15, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
139 units

Product Description

Medline Kits, trays, and packs labeled as follows: a) BREAST PACK, REF DYNJ56344B; b) SEPTOPLASTY PACK WRO-LF, REF DYNJ62803

Reason for Recall

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.

Distribution Pattern

Distribution US nationwide including Puerto Rico, Canada, UAE, and Panama

Code Information

a) REF DYNJ56344B, UDI/DI 40889942612322 (case), 10889942612321 (unit), Lot Numbers: 22CLA043, 22HLA191, 22ILA180, 23BLA030, 23BLB019, 23ELA630; b) REF DYNJ62803, UDI/DI 40193489688994 (case), 10193489688993 (unit), Lot Numbers: 22GBS133, 23GBF930

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-1109-2024
openFDA file date
Oct 6, 2026
Loaded by RegDataLab
Oct 12, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it. FDA may have changed the recall since.