Alfredo Sauce (Del Monaco) – missing allergen label (2013)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Armanino Alfredo Sauce; Frozen in 10 oz x 12 pouches per case (sample, not for retail sale) and 3 lb. pouches 4 x 3 lb. pouches per case for food service use UPC - 10 oz. samples: 10041622 002635 UPC 3 lb. pouch: 10041622 019428 Distributed by Armanino Foods, Hayward, CA; Manufactured by Del Monaco Specialty Foods, Walnut Creek, CA
Brand
Del Monaco Specialty Foods Inc.
Lot Codes / Batch Numbers
Three lots of the 10 oz. pacakges, Packaging Date: 09/24/13 Case code: 0924139438, Package code: A26913 Packaging Date: 09/26/13 Case code: 0926139569
Products Sold
Three lots of the 10 oz. pacakges, and 2 lots of the 3 lb. packages are under recall. The codes for these are as follows: 10 oz. sample size: Product code: 41622 263AS: DSF Code: 960110 Package code: A26713, Packaging Date: 09/24/13 Case code: 0924139438; Package code: A26913 Packaging Date: 09/26/13 Case code: 0926139569; Package code: A31113 Packaging Date: 11/07/13 Case code: 1107131625 4 x 3 lb. pouch size: Product code 41622-1942F; DSF Code 941270 Package code: Use by 9-25-14 Packaging Date:9/25/13 Case code:0925139543 Package code: Use by 11/06/14 Packaging Date: 11/06/13 Case code: 1106131577
Del Monaco Specialty Foods Inc. is recalling Armanino Alfredo Sauce; Frozen in 10 oz x 12 pouches per case (sample, not for retail sale) and 3 due to The product was not labeled with ingredients nor with an allergen declaration; the carton only contained one label which states the product identity b. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product was not labeled with ingredients nor with an allergen declaration; the carton only contained one label which states the product identity by the second label with ingredients and allergen information was inadvertently left off. The product is for food service and is sold in cartons of 4 x 3 lb. individual pouches and samples, not for retail sales.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA
Page updated: Jan 6, 2026