Medical Action Industries, Inc. 306

Frequent Recalls

6

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-05-13 to 2026-09-23

Date	Source	Product	Brand	Severity	Units
2026-09-23	FDA Device	FDA Recall: Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B;	Medical Action Industries, Inc. 306	Class II	N/A
2026-09-16	FDA Device	FDA Recall: Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampule	Medical Action Industries, Inc. 306	Class I	N/A
2026-09-16	FDA Device	FDA Recall: Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Contain	Medical Action Industries, Inc. 306	Class I	N/A
2026-08-12	FDA Device	FDA Recall: Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Cat	Medical Action Industries, Inc. 306	Class II	N/A
2026-08-05	FDA Device	FDA Recall: Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Hand	Medical Action Industries, Inc. 306	Class I	N/A
2026-05-13	FDA Device	FDA Recall: Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case	Medical Action Industries, Inc. 306	Class I	N/A

Medical Action Industries, Inc. 306 Recalls | WatchRecall