Recall archive / FDA device enforcement
Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS, REF CDS983470D; 2) 1/2X1/2 NEURO SPONGE PACK-LF, R... — FDA record Z-0779-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Nov 21, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS, REF CDS983470D; 2) 1/2X1/2 NEURO SPONGE PACK-LF, REF DYNJ0713177; 3) BURR HOLE SHUNT PACK, REF DYNJ56819D; 4) BURR HOLE SHUNT PACK, REF DYNJ56819F; 5) BURR HOLE SHUNT PACK, REF DYNJ56819G; 6) RO VP SHUNT PACK, REF PHS392834010D; 7) VP SHUNT, REF SYNJ10307A.
- Reason
- Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
- Classification
- Class II
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 1402 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0779-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | 1) REF CDS983470D, UDI/DI 10193489275339 (EA) 40193489275330(CS), Lot numbers: 20BDB519, 20EDA360, 20EDC040, 20GDA474, 20JDA107, 20KDA855, 21CDA110, 21EDA674, 21FDA748; 2) REF DYNJ0713177, UDI/DI 10889942085088 (EA) 40889942085089(CS), Lot numbers: 19AKC072, 19HKC645, 19KKA304, 20FKA539; 3) REF DYNJ56819D, UDI/DI 10193489254273 (EA) 40193489254274(CS), Lot numbers: 20AKA332, 20BKA860; 4) REF DYNJ56819F, UDI/DI 10193489353532 (EA) 40193489353533(CS), Lot numbers: 20EKB648, 20HKA426, 20JKA217, 20LKB026, 21FBT545, 21HBL828, 21KBY910, 21KBY914; 5) REF DYNJ56819G, UDI/DI 10195327073749 (EA) 40195327073740(CS), Lot numbers: 22CBJ951, 22HBJ403, 22LBQ584, 23BBH164, 23CBG816, 23FBM524; 6) REF PHS392834010D, UDI/DI 10193489222432 (EA) 40193489222433(CS), Lot numbers: 21LDA084; 7) REF SYNJ10307A, UDI/DI 10193489377026 (EA) 40193489377027(CS), Lot numbers: 20HBU444, 20HBW312, 21EBD895, 21FBE508, 21HBS523. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Worldwide distribution - US Nationwide and the countries of UAE, and Canada.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Jan 8, 2025
- Recall initiation date
- Nov 21, 2024
- Center classification date
- Dec 30, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.