Medical Action Industries Angiography Pack Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Medical Action Industries, Inc. is recalling 657 units of Pack Angiography NCMC due to potential particulate in manifolds that may enter blood circulation.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 13, 2026 and geographically references Arizona, Colorado. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Medical Action Industries, Inc. initiated a voluntary recall of cardiovascular procedure kits containing manifolds that may have particulate within the fluid path, with the potential to be introduced into blood circulation and become lodged within blood vessels.
Which Products Are Affected
Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds. UDI-DI: 20809160490416. Affected lots: 342513 (exp. 1/16/2028), 336758 (exp. 9/20/2027), 338977 (exp. 1/16/2028). Quantity: 657 units. Distributed to AZ and CO.
What You Should Do
Consumers should follow instructions from the recalling firm regarding the affected products.
Why This Matters
The Class I recall involves a potential risk of particulate introduction into blood vessels.
Source
FDA recall number Z-2792-2026, event ID 99337.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (875 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 13, 2026.
Frequently Asked Questions
Common questions about this FDA recall.