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FDA (Device enforcement)Recalled 2024-11-21class ii

MEDLINE INDUSTRIES, LP - Northfield: Medline custom medical procedure kits labeled as: 1) CRANI, REF CDS780089V; 2) CRANIOFACIAL CDS, REF CDS780102K; 3) CRANIOFACIAL CDS, REF CDS780102L; 4) CRANIOFACI

Hazard

Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

Details from the source

Reason for recall: Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination. Distribution: Worldwide distribution - US Nationwide and the countries of UAE, and Canada. Quantity: 474300 units Lot/code info: In sequential order by REF Numbers as listed in product description: REF CDS780089V, UDI/DI 10193489587418 (EA) 40193489587419 (CS), Lot number 19BLA484; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19DBN638; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19EBN450; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19FBN031; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19JBE273; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19JBI710; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 19KBR616; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20BBQ409; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20CBP611; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20EBG877; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20EBS145; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20FBB178; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20FBR886; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 20JBH667; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 21BBJ070; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot number 21DBH746; REF CDS780102K, UDI/DI 10889942714506 (EA) 40889942714507 (CS), Lot num

UPC codes

10193489587418, 40193489587419, 10889942714506, 40889942714507, 10195327251000, 40195327251001, 10195327663636, 40195327663637, 10889942824700, 40889942824701, 10195327051877, 40195327051878, 10195327663407, 40195327663408, 10195327114916, 40195327114917, 10889942611737, 40889942611738, 10193489568424, 40193489568425, 10193489666342, 40193489666343, 10193489354836, 40193489354837, 10193489568448, 40193489568449, 10193489665680, 40193489665681, 10193489355314, 40193489355315, 10195327525231, 40195327525232, 10889942688128, 40889942688129, 10193489242522, 40193489242523, 10195327297824, 40195327297825, 10889942911219, 40889942911210

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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