FDA•Sep 9, 2026CRITICALEpidural/Pain TQC KitMedical Action recalls its Epidural/Pain TQC Kit containing sodium chloride ampules over compromised sterility.2 products
FDA•Aug 3, 2026MODERATEDialysis Change Tray Clear SequenceMedical Action recalls Dialysis Change Tray Clear Sequence (Model 78791) due to improper seal in needle-free access device.
FDA•Jul 30, 2026CRITICALAngiography Procedure Kit ManifoldsAngiography kit manifolds recalled due to particulate risk in blood circulation.
FDA•May 6, 2026CRITICALMedical Action Industries Pack Cath BHHMedical Action Industries is recalling Pack Cath BHH kits due to a potential syringe adapter disconnection issue.
