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FDA (Device enforcement)Recalled 2024-11-18class ii

MEDLINE INDUSTRIES, LP - Northfield: Medline procedure kits labeled as: 1) Port Access Kit, Reorder number CVI5130; 2) VANTEX 7FR 3L 20CM CVC STOCK+ BUNDLE US. Reorder number STCVC01USGV; general surg

Hazard

Certain Medline kits were manufactured and distributed with Procedure Masks with SO SOFT Earloops, and SOFT TOUCH II Surgical Masks which were subsequently recalled for not meeting the bioburden testing requirements of EN 14683.

Details from the source

Reason for recall: Certain Medline kits were manufactured and distributed with Procedure Masks with SO SOFT Earloops, and SOFT TOUCH II Surgical Masks which were subsequently recalled for not meeting the bioburden testing requirements of EN 14683. Distribution: US Nationwide distribution. Quantity: 749 units Lot/code info: 1) CVI5130: UDI/DI 10653160372349 (each) 00653160372342 (case), Lot Numbers: 2024040490, 2024073190, 2024082790, 2024101790,; 2) STCVC01USGV: UDI/DI 10653160376965 (each) 00653160376968 (case), Lot Numbers: 2024050990.

UPC codes

10653160372349, 00653160372342, 10653160376965, 00653160376968

Source

Official record: FDA (Device enforcement)

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

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