Drug recall
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
FDA recall event 98698 · Class I · Medical Action Industries, Inc. 306
Key facts
| Event ID | 98698 |
|---|---|
| Recall numbers | Z-2007-2026 |
| Recalling firm | Medical Action Industries, Inc. 306 |
| Product type | Devices |
| Products | Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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" |
| Initiation date | Mar 17, 2026 |
| Report date | May 13, 2026 |
| City | Arden |
| State | NC |
| Country | United States |
| FEI number | 1030451 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: