Official recall notice

FDA DeviceClass INotable

FDA Recall: Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

Recall date
2026-05-13
FDA class
Class I

Why it was recalled

Hazard

Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"

Recommended action

What to do

2030 kits

Product description

Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"

Verify with the official notice →
Share:

Related Recalls

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
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
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
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