FDA Device recall Z-0788-2025
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-0788-2025 |
| 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 CDS930177C, UDI/DI 10889942810949 (EA) 40889942810940 (CS), Lot Numbers: 19BBO293, 19CBI818, 19EBC020, 19IBS311…1) REF CDS930177C, UDI/DI 10889942810949 (EA) 40889942810940 (CS), Lot Numbers: 19BBO293, 19CBI818, 19EBC020, 19IBS311, 19JBP366, 19LBY043, 19VBE320, 20CBD448, 21ABE744, 21BBN653; 2) REF CDS982054V, UDI/DI 10193489552799 (EA) 40193489552790 (CS), Lot Numbers: 19BBJ530, 19CBL695, 19EBN805, 19EBZ133; 3) REF CDS982683X, UDI/DI 10198459064548 (EA) 40198459064549 (CS), Lot Numbers: 24IBH460; 4) REF CDS982719X, UDI/DI 10198459064531 (EA) 40198459064532 (CS), Lot Numbers: 24IBE288, 24JBB766, 24KBA129; 5) REF CDS983467J, UDI/DI 10195327561116 (EA) 40195327561117 (CS), Lot Numbers: 24ADA818, 24ADC216, 24BDA929, 24DDB447, 24EDA275, 24EDA751, 24GDB213, 24IDA327, 24IDB043, 24IDB372; 6) REF CDS983470C, UDI/DI 10889942730407 (EA) 40889942730408 (CS), Lot Numbers: 19ADC620, 19BDA241, 19CDA866, 19DDA314, 19DDD395, 19FDB295, 19GDA719, 19HDD614, 19JDB841, 19LDB812; 7) REF CDS983470I, UDI/DI 10195327561154 (EA) 40195327561155 (CS), Lot Numbers: 23LDA393, 24ADC171, 24DDA672, 24EDB254, |
|---|
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-0788-2025%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.