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Givaudan Flavours Corp Recall: Positive Salmonella sp. in product

United States

TerminatedClass I

Company
Givaudan Flavours Corp
Product
AY-259-396-6 Nat Chicken (rotisserie) Flavor WONF 18.144kg…
Recall date
October 21, 2021
Terminated
January 20, 2022
Source
FDA

Reason for recall

Positive Salmonella sp. in product

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
AY-259-396-6 Nat Chicken (rotisserie) Flavor WONF 18.144kg packages packaged in brown square boxes with blue plastic interior Not published in this source record 2267.96 kgs Batch No. DV00295989 Catalog No. AY-259-396-9 Expiration date 10/13/22

Distribution

  • 100% of product was shipped to single account in Indiana

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0094-2022
Event ID
88952
Status
Terminated
Classification
Class I
Company
Givaudan Flavours Corp
Product description
AY-259-396-6 Nat Chicken (rotisserie) Flavor WONF 18.144kg packages packaged in brown square boxes with blue plastic interior
Quantity
2267.96 kgs
Reason
Positive Salmonella sp. in product
Recall initiation date
October 21, 2021
Report date
November 10, 2021
Classification date
Not published in this source record
Termination date
January 20, 2022
Distribution pattern
100% of product was shipped to single account in Indiana
UPC, lot, and code information
Batch No. DV00295989 Catalog No. AY-259-396-9 Expiration date 10/13/22
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Givaudan Flavours Corp

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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.