FDA Device recall Z-0782-2025
See DocMan
- FDA Device
- Class II
- ongoing
- Published 2025-01-08
On 2025-01-08 the FDA classified a Class II recall of See DocMan 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-0782-2025 |
| 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
See DocMan
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 CDS981185B, UDI/DI 10884389647141 (EA) 40884389647142 (CS), Lot Numbers: 19CDB151, 19DDD096, 19FDA612, 19IDA540,…1) REF CDS981185B, UDI/DI 10884389647141 (EA) 40884389647142 (CS), Lot Numbers: 19CDB151, 19DDD096, 19FDA612, 19IDA540, 19LDB150, 20BDA647, 20DDB481, 20IDA733, 20LDA459; 2) REF CDS983087G, UDI/DI 10193489237351 (EA) 40193489237352 (CS), Lot Numbers: 21LBS976; 3) REF CDS983302G, UDI/DI 10888277753181 (EA) 40888277753182 (CS), Lot Numbers: 19JDB741; 4) REF CDS983302I, UDI/DI 10193489425659 (EA) 40193489425650 (CS), Lot Numbers: 23FDA273, 23IDA781; 5) REF CDS983483G, UDI/DI 10889942946068 (EA) 40889942946069 (CS), Lot Numbers: 19CDB914, 19DDB938, 19GDB412, 19GDC427, 19JDA647, 19KDB084, 19LDC222, 20BDC250, 20EDB879, 20GDC001, 20JDA007, 20JDB542, 20LDB199; 6) REF CDS983483I, UDI/DI 10193489919585 (EA) 40193489919586 (CS), Lot Numbers: 21FDB817, 21HDA571, 21KDB608, 22BDA109; 7) REF CDS984313G, UDI/DI 10193489540437 (EA) 40193489540438 (CS), Lot Numbers: 19GBL203, 20EBC321, 20KBB606; 8) REF DYNJ0101278F, UDI/DI 10193489352351 (EA) 40193489352352 (CS), Lot Numbers: 20FDA |
|---|
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-0782-2025%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.