FDA Device recall Z-0792-2025
Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B
- FDA Device
- Class II
- ongoing
- Published 2025-01-08
On 2025-01-08 the FDA classified a Class II recall of Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B by Medline Industries Northfield, citing custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0792-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-11-21 |
| Published | 2025-01-08 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B; 2) UROLOGY ROBOTIC, REF DYNJ55555D; 3) KIT,SPINE LH, REF DYNJ906448A.
Reason
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Identifiers
| code_info | 1) REF DYNJ47568B, UDI/DI 10193489846058 (EA) 40193489846059 (CS), Lot Numbers: 21EBP877, 21EBP891, 21GBW057, 21GBW059…1) REF DYNJ47568B, UDI/DI 10193489846058 (EA) 40193489846059 (CS), Lot Numbers: 21EBP877, 21EBP891, 21GBW057, 21GBW059, 21KBG927, 21WBA306, 22ABO417, 22EBE351, 22FBX502, 22FBY332, 22IBJ001, 22LBA177, 23ABD998, 23BBE825, 23CBI861, 23EBO916, 23FBQ324, 23GBN118, 23IBL993, 23JBT331, 23LBC938, 24BBG081, 24BBN421, 24EBC753, 24FBM377, 24HBR212, 24HBS302; 2) REF DYNJ55555D, UDI/DI 23HBQ656; 3) REF DYNJ906448A, UDI/DI 20LBO883, 20WBE707, 21CBS664, 21EBG271. |
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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-0792-2025%22
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