FDAFDA · Food and drugs·Recall number Z-0779-2025
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.
Published January 8, 2025 · Recall initiated: November 21, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- MEDLINE INDUSTRIES, LP - Northfield
- Distributor
- Worldwide distribution - US Nationwide and the countries of UAE, and Canada.
- Lot
- 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.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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