bestemmingsrapport (product)
eindbestemmingsrapport (product)
productstatusrapport (sommige gevallen)

dit komt er denk ik het dichtste bij / in sommige contexten past het helemaal, in andere contexten iets minder

uit een FDA-rapport genoemd:

Chapter 7 RECALL PROCEDURES

Before any FDA approval or concurrence is provided to plans for the disposition of recalled products, .......

If product is to be removed from the market place and recovered, its final disposition should be identified

They will ensure that the firm's status reports are received and reviewed in a timely manner and that the disposition of recalled products is monitored or verified.

FDA will also assign audit checks as appropriate, monitor the effectiveness of the recall communication, correction or removal, verify appropriate product disposition, and terminate the recall

Verbally apprise management that the district office should be consulted prior to the reconditioning or destruction of any returned product. Management should also be advised that FDA must witness or otherwise verify product disposition.

Letters to direct accounts and sub-accounts should include a postage-paid, self-addressed post card, envelope, or other arrangement to enable the consignee to report the amount of the product available and its disposition.

The recall strategy should consider the disposition of recalled products (e.g., carcinogenic products) when normal disposition means, landfill, crushing, denaturing, etc., are inadequate.

It will indicate FDA's determination to verify returned product disposition by stating that the district office should be notified prior to the initiation of reconditioning or destruction of recalled products and that such action should be witnessed by an FDA investigator.


FDA will terminate a recall when the monitoring district office determines that the recalling firm has completed all recall activity, including monitoring and final product disposition


If product is to be removed from the market place and recovered, its final disposition should be identified


Indicate disposition of recalled product:
ڤ returned (specify quantity, date and method)/held for return;
ڤ destroyed (specify quantity, date and method);
ڤ relabeled (specify quantity and date);
ڤ quarantined pending correction (specify quantity);
ڤ transfused – Blood or blood products (specify date and quantity);
ڤ implanted (specify date and quantity)

http://www.fda.gov/downloads/iceci/compliancemanuals/regulat...

interessante koppelingen
deze geven informatie over de bredere context van de vraag

http://www.hc-sc.gc.ca/dhp-mps/compli-conform/prob-report-ra...

http://www.diagned.nl/files_content/Diagned richtlijn vigila...