What's New Unreplied Topics Membership About Us Contact Us Privacy Policy
[Ad]

Does anyone have a hold and release form?

Started by , Mar 10 2015 05:23 PM
3 Replies

Does anyone have a hold and release form, damaged inventory and product return form sample they would like to share?

Share this Topic
Topics you might be interested in
FSSC 22000 Announce the Release of FSSC Development Program V2.0 Using FSIS Form 7234-1 for Generic Label Approvals Internally What Information Should Be Included in a Hold-Release and CAPA Document? Improving Final Product Release Process What does BRCGS say about hold material?
[Ad]

Hi,

 

Wish I had a sample form,but I can at least give you a start on what it should address. Maybe others have more and better ideas they might contribute. Going from memory:

 

Place for current date/time (time is critical data to capture because if it is an out-of-temperature range issue, knowing and documenting the times is crucial to decisions)

 

Who put it on HOLD

 

Exact description include prodcut/ingredient name, LOT number(s)

 

Exact quantity involved, number of units, pounds, gallons, pallets

 

Is it a food safety issue vs. a quality issue

 

Exact description of suspected problem - misformulation, contamination, mis-labeled, out of temperature, out of specification

 

Initial actions taken - waiting on lab results, reprinting labels, placed in blast freezer for fast temperature reduction, product is in process e.g. being tempered, extraneous matter found

 

corrective actions, preventative actions, root cause analysis

 

Was there a deviation from the critical limits of a critical control point?

 

final disposition - destroyed, witnessed by USDA, donated to charity, reworked into product x with LOT number x

 

Estimate the date of resolution/finalization

 

Decision making documents

Reference related documents

 

Release time and date

 

Authorization signatures

 

I hope this may assist with ideas anyway. Return to warehouse documents will be similar. Such documents need to answer who, what, why, when and where. They need to carry justification for actions, proper authorization(s), due diligence, clear paper trail, etc.

 

Regards,

 

Xylough

3 Thanks

Hi,

 

As much as I agree with what is in the post above IMHO I feel it is also important to realise what standard you are working to / which industry you are in.

Relevant standard requirements will then tell you what must be included in your Hold/Release procedure.

What can also be done is linking the Hold to Non-Conforming Materials procedure (and applying the adequate category within NCR's).

This will allow you to keep all details of investigation within the NCR document, not necessary have it written on the Hold form attached to the product itself. Saves the space on the form and allows the Hold form to send a clear message to all staff: wait a minute we shall not be using this.

We have a log (simple spreadsheet) of all Held products/materials/packaging/obsolete packaging/WIP containing all details as per above post and on the actual Hold notice attached to the product we would put Hold number as an identification.

Details of all actions taken can then be found in the log.

Let's not forget about having the internal document control references added to the form and the need for having a designated area - Quarantine area to keep all products but again - this may be interpreted differently depending on which standard you are working to.

 

Regards

1 Thank

Hello knd12288,

         Attached are some forms which may be of help to you.

Attached Files

17 Thanks

Similar Discussion Topics
FSSC 22000 Announce the Release of FSSC Development Program V2.0 Using FSIS Form 7234-1 for Generic Label Approvals Internally What Information Should Be Included in a Hold-Release and CAPA Document? Improving Final Product Release Process What does BRCGS say about hold material? Ingredient statement when using a dry form of an ingredient Manufacturer Input form & Food Chain ID Standard Ingredient Form Product testing during release as a CCP Releasing Product Prior to Positive Release Being Completed for Customer Is there any method available for Cold filled and Hold process parameters