Class ITerminated in FDA datasetRecall initiated Oct 21, 2015

DH. ANCHOVY 2.2 Lbs.; Item No: D0161; B/C: 59033 50161; DH. ANCHOVY 3.5 oz..; Item No: D0162;…

Recalling firm: Seafood Avenue

Why it was recalled

Product may have the potential for pathogen growth and toxin formation due to Clostridium botulinum.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 27, 2017.

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ProductDH. ANCHOVY 2.2 Lbs.; Item No: D0161; B/C: 59033 50161; DH. ANCHOVY 3.5 oz..; Item No: D0162; B/C: 59033 50162
Package size2.2 Lbs

FDA code information

Lot Codes: TTL-D1615 and TTL-H0715; Lot Codes: TTL-L1014 and TTL-K2814

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Full FDA record and distribution details

Original product description

DH. ANCHOVY 2.2 Lbs.; Item No: D0161; B/C: 59033 50161; DH. ANCHOVY 3.5 oz..; Item No: D0162; B/C: 59033 50162

Original FDA recall reason

Product may have the potential for pathogen growth and toxin formation due to Clostridium botulinum.

Recall details

Recall number
F-1743-2017
Event ID
72473
FDA status
Terminated
Initiated
Oct 21, 2015
Reported
Apr 5, 2017
Classified
Mar 27, 2017
Terminated
Mar 27, 2017
Quantity
490 units
Location
El Monte, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

CA, PA, CO, IL, WI, MA, TX, MD, MI, MN, UT

FDA source record · F-1743-2017

Data updated September 16, 2026. View official FDA data ↗

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