SAF Pro Relax Yeast (Aveka Nutra) – Metal Contamination (2018)
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
SAF PRO RELAX +YF, Deactivated Dry Yeast, Product Code 73050, Net Wt. 50 LBS. (22.7 KG), manufactured for Lesaffre Yeast Company, Milwaukee, WI.
Brand
Aveka Nutra Processing
Lot Codes / Batch Numbers
Lot#: T110817A, expiration date: 11/8/18, T110917A, expiration date: 11/9/18, T111017A, expiration date: 11/10/18, T111117A, expiration date: 11/11/18, T111217A, expiration date: 11/12/18, T111317A, expiration date: 11/13/18, (Bag# 1-76), and T111317B
Products Sold
Lot#: T110817A, expiration date: 11/8/18; T110917A, expiration date: 11/9/18; T111017A,expiration date: 11/10/18; T111117A, expiration date: 11/11/18;T111217A, expiration date: 11/12/18; T111317A, expiration date: 11/13/18; (Bag# 1-76), and T111317B
Aveka Nutra Processing is recalling SAF PRO RELAX +YF, Deactivated Dry Yeast, Product Code 73050, Net Wt. 50 LBS. (22.7 KG), manufacture due to Product has potential to be contaminated with pieces of metal.. 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
Product has potential to be contaminated with pieces of metal.
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
IN, IA
Page updated: Jan 6, 2026