DeviceSignal · Recall classified
Medical Action Industries, Inc. 306
FDA classified a device recall on 2026-07-30 · Class I · Z-2792-2026
EventRecall classified
Effective2026-07-30
ClassificationClass I
On 2026-07-30 the FDA classified a device recall from Medical Action Industries, Inc. 306 as Class I. Product: Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic…. Recall Z-2792-2026. The firm initiated it on 2026-05-13. This reports the classification FDA published on that date.
Reported facts
- Recall number
- Z-2792-2026
- Classification
- Class I
- Classified on
- 2026-07-30
- Initiated on
- 2026-05-13
- Firm
- Medical Action Industries, Inc. 306
- Reason
- 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
- Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_enforcement
- Source record
Z-2792-2026- Snapshot hash
ab5ada73bf212eb52a548aab0968a0fcee42807c61b0350e60e24bb6e2beed72- Source URL
- https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
- Observed
- 2026-09-08T16:22:09.483Z
- Transform
fda_device_enforcement_to_recall v1- Event rule
fda_device_recall_classified v1- Event key
41ece3b654ca474164153df9e425f3b41d95c0dcf49b20bed44336f64728c1b2- Signal type
device_recall.classified
Source terms that apply
- This is not a public alerting service and must not be used to notify patients or the public
- We do not report whether a recall is still open; FDA does not maintain that after classification
- Nothing here is a medical or clinical decision aid
- Not affiliated with, endorsed by, or certified by the FDA
Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)