Required documents for FDA Withdrawal or Recall?
Started by ncwingnut, May 30 2019 08:22 PM
Good afternoon, all!
Does anyone know if there is a published list or templates of the documentation required by the FDA for a recall or withdrawal? I'm thinking I saw some templates on the FDA site a few years ago, but I may be confusing with something else.
Am updating our recall program and would like to include them.
Any help appreciated!
Lynn
SQF-2.4.8 - Is an Environmental Program Required?
Quarterly Goals – Required Sign-Off Authority
SQF Recall Training – Is Coverage on All Shifts Required?
Required Room Temperature Range for Shelf-Stable, RTE Thermally Processed Products
Is Scientific Literature Enough for ISO 22000 Validation, or Is Practical Testing Required?
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The FDA recently updated their web site, so some of their own links aren't valid anymore. I found this site which appears to have the information you are looking for.
https://www.fda.gov/...uidance-recalls
Hopefully it helps.
Thanks,
Todd
SQF-2.4.8 - Is an Environmental Program Required?
Quarterly Goals – Required Sign-Off Authority
SQF Recall Training – Is Coverage on All Shifts Required?
Required Room Temperature Range for Shelf-Stable, RTE Thermally Processed Products
Is Scientific Literature Enough for ISO 22000 Validation, or Is Practical Testing Required?
SQF 2.4.5 & 2.6.2.1 - Is Lot Tracking Required for Recouped Beverages
Is SOP Author Training Required? Clarification on NR Received
Is Air Testing required if the compressed air we use is only for the machines?
Are Storage Conditions Required on Labels by FDA-USDA?
Is Additional USDA Label Approval Required for Origin Statement Changes?