Puredesi Whole Milk Yogurt in
Reason yogurt that was produced on 2 different dates (February 23, 2016 and February 29, 2016) in which the hold time was not held for the proper length of time to meet the requirements of pasteurization.
Puredesi Low Fat Yogurt in recall
Recalled by JRZ Dairy Products Inc. · Selinsgrove, PA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
yogurt that was produced on 2 different dates (February 23, 2016 and February 29, 2016) in which the hold time was not held for the proper length of time to meet the requirements of pasteurization.
These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.
What was recalled
Puredesi Low Fat Yogurt in 2 lb. plastic containers Puredesi Low Fat Yogurt in 5 lb. plastic containers Puredahi Low Fat Yogurt in 2 lb. plastic containers
Quantity: 176 - 2lb. containers Puredesi; 156 - 5lb. containers Puredesi; 200 - 5lb Puredahi.
Food: Milk & dairy
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Sell by 5/12/2016
Where it was sold
New Jersey
FDA's distribution note: Central NJ
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- JRZ Dairy Products Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 4, 2016
- In FDA report of
- Apr 20, 2016
- Terminated
- Jun 26, 2017
- FDA recall number
- F-1035-2016 · event 73462
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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