Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 21, 2023 (3 years ago)

Vital Proteins Collagen Peptides recall

Recalled by Vital Proteins · Franklin Park, IL, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

potential foreign material contamination (pieces of one blue broken lid may be in one or more canisters)

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

Vital Proteins Collagen Peptides, retail 24oz plastic canister, UPC 8 57273 00866 6; 6 retail units per wholesale case

Quantity: 59,701 canisters

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.

30095993HA Best By: 01-09-2028

Where it was sold

Alabama Connecticut Delaware Florida Georgia Iowa Illinois Indiana Massachusetts Missouri Mississippi North Carolina New Hampshire New Jersey New York Pennsylvania Puerto Rico South Carolina Tennessee Vermont Wisconsin

FDA's distribution note: Distributed to retail locations in the following states: Iowa Illinois Indiana Missouri Wisconsin Connecticut Delaware Massachusetts New Hampshire New Jersey New York Pennsylvania Vermont Alabama Georgia Mississippi North Carolina South Carolina Tennessee Florida Puerto Rico Online by Consignee.

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
Vital Proteins
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 21, 2023
In FDA report of
Jun 7, 2023
Terminated
Oct 7, 2024
FDA recall number
F-0969-2023 · event 92242
Official record
FDA enforcement report search