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Crown Prince, Inc Recall: Detectable levels of Per- and polyfluoroalkyl substances (PFAS).

United States

TerminatedClass II

Company
Crown Prince, Inc
Product
Crown Prince Quality Natural Seafood Smoked Baby Clams Hand…
Recall date
July 15, 2022
Terminated
November 21, 2022
Source
FDA

Reason for recall

Detectable levels of Per- and polyfluoroalkyl substances (PFAS).

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Crown Prince Quality Natural Seafood Smoked Baby Clams Hand Packed in Olive Oil From Managed Fisheries NET WT. 3 oz. (35g) UPC 0 73230 00853 5 Not published in this source record 211,716 cans All lot codes associated with can UPC 0 73230 00853 5

Distribution

  • U.S. distribution to the following: nationwide. No foreign distribution.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1551-2022
Event ID
90613
Status
Terminated
Classification
Class II
Company
Crown Prince, Inc
Product description
Crown Prince Quality Natural Seafood Smoked Baby Clams Hand Packed in Olive Oil From Managed Fisheries NET WT. 3 oz. (35g) UPC 0 73230 00853 5
Quantity
211,716 cans
Reason
Detectable levels of Per- and polyfluoroalkyl substances (PFAS).
Recall initiation date
July 15, 2022
Report date
August 24, 2022
Classification date
Not published in this source record
Termination date
November 21, 2022
Distribution pattern
U.S. distribution to the following: nationwide. No foreign distribution.
UPC, lot, and code information
All lot codes associated with can UPC 0 73230 00853 5
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Crown Prince, Inc

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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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.