Class IITerminated in FDA datasetRecall initiated Oct 29, 2021

TK006 Van Krimpet Powder Blend 50#. Item number 4107780

Recalling firm: Puratos Corporation (HQ and Innovation Center)

Why it was recalled

Product may be contaminated with foreign material (metal)

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: Aug 28, 2023.

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ProductTK006 Van Krimpet Powder Blend 50#. Item number 4107780

FDA code information

Batch Numbers 0010636568 and 1110644921,

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Full FDA record and distribution details

Original product description

TK006 Van Krimpet Powder Blend 50#. Item number 4107780

Original FDA recall reason

Product may be contaminated with foreign material (metal)

Recall details

Recall number
F-0248-2022
Event ID
89006
FDA status
Terminated
Initiated
Oct 29, 2021
Reported
Dec 8, 2021
Classified
Dec 6, 2021
Terminated
Aug 28, 2023
Quantity
30,350 lbs
Location
Pennsauken, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distributed to domestic customers in CA, NJ, IN, PA, TN, NY, NC, TX, FL, DE, LA, and LA. Distributed to foreign customers in Dominican Republic and Trinidad.

FDA source record · F-0248-2022

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

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