FDA Medical devices recall ·
Medical Action Industries Inc recall
This is an FDA Class I recall — the most serious type.
- Recall number
- Z-2007-2026
- Date
- (initiated March 17, 2026)
- Company / brand
- Medical Action Industries, Inc. 306
25 Heywood Rd, Arden, NC, United States - Category
- Medical devices › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 2030 kits
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Why was it recalled?
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 should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789
Distribution
US distribution to state of: AZ OUS: None
States: Arizona
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (medical devices), recall Z-2007-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.