Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Reason for recall: Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension. Distribution: US Nationwide distribution Quantity: 315 units Lot/code info: UDI/DI 10888277395374, Lot Numbers: 506894, 509420, 512983, 513469, 514448, 514549, 515557, 515860, 515903, 516550, 517359, 517626, 519259, 519413, 519966, 520277, 521360, 522144, 522145, 525472, 527111, 527115, 527121, 528456, 528457, 528582, 529483, 529485, 529487, 529489, 529930, 530432, 530433, 530434, 531020, 531024, 531676.
10888277395374
Official record: FDA (Device enforcement) ↗
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