Recall Z-2007-2026— Medical Action Industries, Inc. 306
Class I · Ongoing
Class I FDA medical device recall by Medical Action Industries, Inc. 306, initiated 2026-03-17. FDA's recall record names no specific 510(k) clearance for this event. Product: Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case. Reason: 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".
- Recalling firm
- Medical Action Industries, Inc. 306
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2026-03-17
- Firm location
- Arden, NC, United States
Product description
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Reason for recall
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"
Data sourced from openFDA. This site is unofficial and independent of the FDA.