CLASS I ONGOING Device recall · Reported 5 Aug 2026 · FDA Enforcement Report
Pack Angiography Ncmc 3/Cs Banner recalled by Medical Action Industries
Medical Action Industries Inc. 306 is recalling Pack Angiography Ncmc 3/Cs Banner, distributed in Arizona, Colorado. The recall was initiated on 13 May 2026 and the FDA has classified it as Class I.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2792-2026
- FDA event ID
- 99337
- Recalling firm
- Medical Action Industries Inc. 306, Arden, NC
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 13 May 2026
- FDA classified
- 30 Jul 2026
- Reported
- 5 Aug 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- N/A
- Reason category
- Particulate Matter
- Device type
- Other Medical Devices
Timeline
| 13 May 2026 | Recall initiated by company | |
| 30 Jul 2026 | Classified by FDA | +78 days |
| 5 Aug 2026 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within blood vessels.
Product as listed by the FDA
Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
Where it was distributed
US: AZ, CO
Questions about this recall
Why was it recalled?
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within blood vessels.
Which lots are affected?
UDI-DI: 20809160490416. Lot/Expiration: 342513(1/16/2028), 336758(9/20/2027), 338977(1/16/2028)
Where was it sold?
US: AZ, CO
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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