Updated: April 2026

Angio pack recall: what to check + what to document

If you’re trying to figure out whether a kit/component you have is included in an FDA recall notice, the hardest part is usually the admin: identifying the exact item, capturing the right identifiers, and keeping a clean timeline.

Educational only. This page is not medical advice and does not replace guidance from a licensed clinician, facility policy, your supplier, or the official recall notice.

Fast first step: identify the exact product (don’t rely on memory)

In recall situations, small details matter: product name, catalog/reference numbers, lot numbers, serial numbers, and the specific component name (not just the “kit”).

Do this now: take 3 photos in good light: (1) full outer packaging label, (2) close-up of lot/serial identifiers, (3) any insert/IFU page that shows product codes.

What to check (the 60‑second checklist)

  • Product / component name (exact wording on the label)
  • Manufacturer / distributor
  • Catalog / reference number (REF, catalog #, item #)
  • Lot number (and/or serial number if present)
  • Expiration date (if shown)
  • UDI (Unique Device Identifier) barcode text, if available
  • Quantity on hand (how many units, where stored)

What to document (so follow-ups are actually doable)

For logistics and audit trails

  • Where it came from (supplier, facility, department)
  • Purchase order / invoice number (or screenshot)
  • Date received and where it was stored
  • Who you notified and when (names + timestamps)

For “what happened” notes (keep it factual)

  • Any relevant event dates/times (e.g., when the kit was opened/used)
  • Which room/procedure context (high-level, no sensitive details)
  • What you observed (plain description, no conclusions)
Safety note (non‑medical): follow the official recall instructions for your setting (home, clinic, hospital). If a notice mentions exposure risk, your next steps should come from the recall notice and your facility’s safety process.

How Jabbit helps in recall situations

  • One place for photos, identifiers (REF/lot/serial/UDI), and vendor paperwork.
  • A clean timeline so you can answer “what did we have, when did we learn, what did we do?”
  • Follow‑up reminders so callbacks and replacement requests don’t slip.

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