For Compliance & Safety

Be ready before the notice arrives.

When a product safety issue occurs, your team needs to establish what was affected, where it went, what remains on hand, and what action was taken. iPothecary gives compliance and safety teams a connected operational record to investigate and coordinate the response without starting from scratch.

The Reality

The questions arrive immediately. The answers shouldn't require an investigation.

When a recall is announced, compliance teams face a sequence of urgent questions in rapid succession.

What product is affected? Which manufacturer, which NDC, which lot?
Which of our offices received this product — and when?
How much of the affected lot is still on shelves?
Was any of it sold? To whom?
Has affected inventory been removed from use?
What action was taken, by whom, and when?
Can we document the response if we're asked to demonstrate it?

Without a structured system, the investigation starts from scratch — with phone calls, spreadsheet lookups, and manual cross-referencing across purchasing records, POS exports, and paper logs. iPothecary provides the operational record that connects these answers before the recall arrives.

Traceability when it matters most

The recall workflow, step by step.

iPothecary helps trace a recall from announcement through documented response. Every step below represents information that exists in the system because the operational record was built from day one.

Safety event announced

FDA recall notice or manufacturer safety communication received. Product identified by name, NDC, lot number, or UPC.

01

Product matched in catalog

Search the iPothecary catalog by NDC, UPC, product name, or manufacturer. Identify the exact product and package associated with the recall.

02

Affected lots identified

All received inventory for the product is tracked by lot number and expiration. The affected lot is matched against receiving records across all locations.

03a

On-hand inventory located

Which offices received the affected lot. How much remains on hand. How much is already committed or reserved.

04a

Hold placed on affected stock

Inventory quarantined across affected locations. Removed from available quantities. Recall hold documented with timestamp and responsible party.

03b

Prior sales surfaced

Where transaction records are available, review sales involving the affected lot, including date and location, to support appropriate outreach.

04b

Customer records available for outreach

Where patient contact information exists, it can be used to support outreach. Outreach actions are tracked separately from the inventory response.

05

Response documented

Every action — hold placement, inventory disposal, customer outreach, lot disposition — is timestamped and attributed. The response record exists whether or not it is ever reviewed.

Traceability Infrastructure

What makes the recall response possible

Lot-level receiving records

Every received shipment records lot number, expiration date, vendor, and purchase order. Lot traceability begins at the point of receiving, not during the investigation.

Product identification

The product catalog includes manufacturer, NDC, UPC, and package identifiers. A recall identified by NDC can be matched to a catalog product and all related inventory.

Multi-location inventory holds

Inventory holds can be placed across all locations simultaneously. Held stock is removed from available quantities and flagged for review or disposal.

Transaction history by lot

Transaction records identify which sales involved a specific lot, by location and date. Where patient information exists, it is accessible for outreach decisions.

Documented activity history

Inventory movements, holds, adjustments, and disposals can be recorded with timestamps and responsible users for later review.

Manufacturer information

Manufacturer and vendor information is part of the product record — not stored separately. A recall from a specific firm can be tied back to which products and lots came from them.

What iPothecary does and doesn't do

iPothecary helps identify affected inventory, helps document the response, and provides traceability that supports established recall workflows. It does not automatically satisfy recall requirements, guarantee regulatory compliance, or replace your organization's own safety and quality processes. Compliance decisions remain with your team.

What it does provide is the operational record that ensures the investigation doesn't start from scratch — because the traceability was built into day-to-day operations from the beginning.

Everyday product safety

Safety doesn’t begin and end with a recall.

Expiration exposure, questionable stock, product identity, holds, and disposition are part of the same operational discipline that makes exceptional events easier to investigate.

Identify aging and expiring inventory.
Remove questionable stock from availability while it is reviewed.
Keep product and package identifiers connected.
Document what ultimately happened to held or affected product.

Implementation readiness

Recall readiness starts before the recall.

Implementation can help your organization define notice recipients, inventory holds, inspection responsibilities, escalation paths, and response documentation before a safety event occurs.

  • Notice recipients and escalation
  • Site inspection and affected-stock workflows
  • Lot, expiration, hold, and disposition records
  • Staff roles, training, and response documentation

When something goes wrong, don't start from scratch.

Request a walkthrough of the recall and traceability workflows for your organization.