Medical Action Industries Pack Cath BHH
Pack Cath BHH contains a syringe whose rotating adapter may unwind, causing loose or full disconnection.
High risk
There is a reasonable chance that using it could cause serious health problems or death.
FDA Class I recall · How risk is rated
What happened
Medical Action Industries, Inc., of Arden, North Carolina, recalled its Medical Action Industries Inc. Pack Cath BHH convenience kit, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case, because the 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. The recall began on March 17, 2026, and was added to the FDA's Enforcement Report on May 6, 2026.
The recalled kits were distributed in the state of Arizona, with no distribution outside the United States. The recall involved 2030 kits.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the UDI-DI and lot code listed under your product.
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
- UDI-DI
- 20809160490294
- Lot
- 342509
- 346066
- 338434
- 339423
- 337365
- 335489
- 336189
- 336789
Details
- Company began the recall
- Sold in
US distribution to state of: Arizona OUS: None
- Event ID
- 98698
- Recall No.
- Z-2007-2026
- Company
- Medical Action Industries, Inc. 306Arden, North Carolina
- Hazard
- Device defect
- Quantity recalled
- 2030 kits
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
