FDA recall record

Niagara Bottling Limited Edition Winter Mint Chocolate Premier Protein 30g recall — FDA F-0382-2023

The recalled product did not meet the pre-kill step processing specifications and has the potential to be spoiled.

Class IIclassification
F-0382-2023official record ID
Mar 8, 2023report date

Recall record at a glance

Official recordF-0382-2023
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNiagara Bottling
Report dateMar 8, 2023
Recall initiation dateFeb 14, 2023
Quantity1152 cases
LocationDiamond Bar, CA, United States

Official product description

Limited Edition Winter Mint Chocolate Premier Protein 30g Protein High Protein Shake 11.5oz (340mL) UPC 00643843801498 packaged in plastic bottles in full wrap lithographpacked in a cardboard case, 12 packages per case

Why the product was recalled

The recalled product did not meet the pre-kill step processing specifications and has the potential to be spoiled.

Distribution information

CA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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.

Related recall records

Other records from the same recalling company are shown first when available.