Romaine lettuce packaged into the following configurations and sizes recall

Recalled by G.O. Corporation · Minneapolis, MN, United States

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

Why it was recalled

Romaine lettuce may be contaminated with deer feces.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Romaine lettuce packaged into the following configurations and sizes: 1. Lettuce Romaine Shred, Produce Code 720325, 4-2.5lb. bags per shipping case, Customer UPC 9120457. 2. Romaine Shred 1/4", Produce Code 720425, 4-2.5lb bags per shipping case, Customer UPC 7641269 and 8095202. 3. Lettuce Romaine Shred, Produce Code 720449, 8-2.5lb.bags per shipping case, Customer UPC 7166295 and 7599586. 4. 1.5XRandom, Produce Code 720625, 4-2.5lb bags per shipping case Customer UPC 1672815. 5. 1.5XRandom, Produce Code 720725, 4-2.5lb bags per shipping case, Customer UPC 1855196 and 8950701. 6. 1.5XRandom, Produce Code 720732, 6-2lb bags per shipping case, Customer UPC 3179397 and 4106811. 7. 1.5XRandom, Produce Code 720747, 3-2lb bags per shipping case, Customer UPC 3100922. 8. Medium, Produce Code 720832, 6-2lb per shipping case, Customer UPC 5087588. 9. Medium, Produce Code 720840, 10-2lb per shipping case, Customer UPC 720840.

Quantity: 23,186 lbs. total

Food: Leafy greens & salads

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.

Lot Codes: 1. 130208, 130209, 130212; 2. 130208, 130209, 130212; 3. 130209; 4. 130209, 130212; 5. 130209, 130212; 6. 130209, 130212; 7. 130209, 130212; 8. 130209, 130212; 9. 130212.

Where it was sold

Iowa Minnesota North Dakota Wisconsin

FDA's distribution note: IA, MN, ND, WI

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.

Recalling firm: G.O. Corporation
Initiated by: Voluntary: Firm initiated
Recall initiated: Aug 1, 2023
In FDA report of: Aug 23, 2023
FDA recall number: F-1423-2023 · event 92828
Official record: FDA enforcement report search

Also recalled with it (7 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Ongoing Other Aug 1, 2023