Dear Doobey,
Interesting topic. In my country, there is no mandatory regulation that manage the traceability and withdrawal procedures. The goverment only gives ultimatum to companies to withdrawn their products when the National Agency of Food and Drugs Control found nonconformities, but they dont direct how the withdrawal procedures should be.
As for the traceability and withdrawal procedures, every company has it own ways, depend on system that they use. Mostly, in here we are still counting system from ISO 9001 and ISO 22k. As for myself, I am adapting the ISO 22k system. We have two kind of treacebility:
1. Tracing: we trace where a non conformance Raw Material goes to (WIP or products), this part is harder, because we have so many kind of WIP and products.
2. Tracking: we track a non conformance FG from customer. From it batch number, we can track every Raw Material and their batch number, so we can define what material or process that has nonconformance. This is easier, because we are focusing only to one products. But if the non conformance material goes to many products, thats what I call troublesome...
However, when a Star Yum! auditor came visit us last May, somehow we manage to clear them in two hours, manually... Its quite annoying...
For the withdrawn procedure, I hate when we have to do simulation if a non conformity products went to the distributor. Because we have to found every single customer that demanding products from our distributor. Its a big pain in the a**.
Regards,
Arya