Recall record at a glance
| Official record | F-0017-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Mothers' Milk Bank of Montana |
| Report date | Oct 15, 2014 |
| Recall initiation date | May 13, 2014 |
| Quantity | 354 fl oz |
| Location | Missoula, MT, United States |
Official product description
Frozen Unpasteurized Human Milk in glass bottle. No labeling provided
Why the product was recalled
Donor answered NO to question #32 "In the last 28 days, have you ever had a vaccine for measles, mumps or rubella?" It was later discovered that she had in fact received live vaccines for influenza, DTAP and MMR after delivery.
Distribution information
354oz bottle of unpasteurized milk was transfered to Mother's Milk of San Jose, CA. 12 - 4oz bottles was delivered to Community Medical Center, Missoula, Montana.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.