Recall Ledger

Medical Action Industries Inc. Pack Cath BHH recall (Medical Action Industries, Inc. 306)

Medical deviceClass IOngoing

Summary: Medical Action Industries, Inc. 306 is recalling 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".

What is being recalled

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

Why

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"

How serious is it

Class I is the most serious level: FDA considers there is a reasonable probability that using or being exposed to this product will cause serious health problems or death.

Where it was sold

US distribution to state of: AZ OUS: None (states named: Arizona)

How to tell if yours is affected

UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-2007-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass I
StatusOngoing
Recall startedMarch 17, 2026
ReportedMay 13, 2026
CompanyMedical Action Industries, Inc. 306
Company locationArden, NC, United States
Initiated byVoluntary: Firm initiated
Quantity2030 kits

More recalls from Medical Action Industries, Inc. 306 · all medical device recalls · recalls from March 2026

Official FDA record