Current FDA corpus
Try an official recall number, a recalling firm, or a phrase from the source record.
Device evidence
REF: B90240-50, 96" (244 cm) Appx 11.2 ml, 10 Drop Admin Set w/Coiled Tubing, Pre-Slit Port, Clave, Rotating Luer, Sterile R, UDI: (01)00887709077058
Official recall number
Z-1913-2020
Field note
We'll only use this to respond to your feedback.