Horizon Organic ORG ASEP CHOC MILK 1%
Reason Product has the potential to be spoiled.
Mountain West Mothers' Milk Bank recall
Recalled by Mountain West Mothers' Milk Bank Inc. · South Salt Lake, UT, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Foreign object found in bottle.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
Mountain West Mothers' Milk Bank - Pasteurized Donor Human Milk, 3 fluid ounce BPA free plastic bottles, embossed with "Donor Human Milk" and graduation marks on the front side Unique identifier label which includes distributing Milk Bank Code (MWMMB), Batch ID, Unique Bottle number, Expiration Date, QR Code, Total Calorie content (kcal./oz), Fat content, Protein Content, and Calculated Lactose. EXP: 09/01/2021 Store at or below -18 C until ready to thaw for dispensation for baby feed. Unique QR code per bottle.
Quantity: 140 - 3 oz. BPA free plastic bottles
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.
Batch 000955-1 Batch 000955-2 Batch 000955-3 Batch 000955-4 All batches expire: 9/1/2021
Where it was sold
Utah
FDA's distribution note: Utah - Salt Lake County, Utah County.
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
- Mountain West Mothers' Milk Bank Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 13, 2021
- In FDA report of
- Apr 28, 2021
- Terminated
- Apr 22, 2022
- FDA recall number
- F-0460-2021 · event 87740
- Official record
- FDA enforcement report search
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