Class IIITerminated · reported 2013-02-06

WP Saki Ika Cuttlefish Hot JFC# 15606, 4/24/0.75 oz; JFC# 06318, 8/12/2 oz; JFC# 07269…

J F C International Inc recalled this product and the FDA reported the enforcement action on 6 February 2013 as Class III. The recall was initiated by the firm. JFC International is recalling WelPac Saki Ika Cuttlefish because of mold.

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product
WP Saki Ika Cuttlefish Hot JFC# 15606, 4/24/0.75 oz; JFC# 06318, 8/12/2 oz; JFC# 07269, 5/12/4 oz; JFC# 06360, 3/12/8 oz.
Reason for recall
JFC International is recalling WelPac Saki Ika Cuttlefish because of mold.
Firm location
Los Angeles, California, United States
Classification
Class III
Status
Terminated
Recall number
F-0951-2013
Quantity
500 cartons
Distribution
nationwide in the US
Initiated
31 October 2012
Reported by FDA
6 February 2013
Terminated
14 February 2013
Firm notified by
Letter
Product codes
JFC# Lot# 15606 Q069A & Q110A; 06318 Q068A & Q111A; 07269 Q070A & Q112A; 06360 Q069A & Q112A.

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

  • Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
  • The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
  • This is one of 2 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. All 2 of them are listed on this page.
  • The recall ran for 3 months, from 31 October 2012 to termination on 14 February 2013. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
  • The FDA published the enforcement report 3 months after the firm began the recall.
  • The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.

What this recall was for

Spoilage and mould

A spoilage recall means the food degraded before its date: mould growth, unintended fermentation, swelling or rancidity, usually traced to a seal, a formulation or a storage temperature.

A preventive controls plan covers spoilage under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.

21 CFR 117.93
Warehousing and distribution: storage and transport under conditions that protect food against contamination and against deterioration of the food and its container.
21 CFR 117.80(b)(3)
Time and temperature: holding food at temperatures that do not allow microorganisms to grow, and for no longer than the process allows.

Every product in this recall

The FDA opened 2 enforcement records for this one recall, one per product code. This page carries all of them; the 1 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.

The other 1 records of FDA event 63978
ReportedProductFirmReasonClass
2013-02-06WP Saki Ika Cuttlefish JFC# 15603, 4/24/0.75oz; JFC# 06315, 8/12/2oz; JFC# 07266, 5/12/4oz; JFC# 06375, 3/12/8oz.J F C International IncJFC International is recalling WelPac Saki Ika Cuttlefish because of mold.Class III

Other records from J F C International Inc

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 18 other records name this firm.

ReportedProductFirmReasonClass
2024-09-04J-Basket Brand, Napa Kimchi, Net Wt. 14.1oz. plastic jar container (12 jars per case).J F C International IncHigh levels of Yeast growth and film on top of jarred Kimchi product.Class II
2021-12-08WEL-PAC Brand Shrimp Dashi No Moto - Powdered Shrimp Stock; Net Wt. 1.75 oz. (0.35.oz x 5 bags) 49.6 g UPC: 0 11152 83660 7 Product of Japan; Imported by JFC International Inc., Los Angeles, CA 90040 INGREDIENTS: SALT, MONOSODIUM GLUTAMATE, SUGAR, GLUCOSE, SHRIMP EXTRACT POWDER (TAPIOCA, SWEET POTATO, CORN, SHRIMP, MONOSODIUM GLUTAMATE, SALT, BEET, SOYBEAN, DISODIUM SUCCINATE), SHRIMP POWDER, CORN OIL, DISODIUM SUCCINATE, DISODIUM INOSINATE AND DISODIUM GUANYLATE, CITRIC ACID, MIXED SEASONING (MONOSODIUM GLUTAMATE, DISODIUM SUCCINATE, DISODIUM INOSINATE AND DISODIUM GUANYLATE, HYDROLYZED PROTEIN (CORN, WHEAT, SOYBEAN, TAPIOCA), DEXTRIN, SALT, SUGAR, POTATO STARCH). CONTAINS: CRUSTACEAN SHELLFISH (SHRIMP), SOYBEAN, WHEATJ F C International IncManufacturer notified US supplier that powdered shrimp stock did not declare fish (hydrolyzed protein that contains bonito, sardine and tuna), on the label.Class I
2021-04-21J-Basket Premium Korean Seaweed Snack - Wasabi flavor on outer wrap for 3 inner packages Inner packages labeled J-Basket Premium Seaweed Snack - Original. Net Wt 0.52 oz. (15g) 3-0.17 oz. (5g) packs Distributed by JFC International Inc., Los Angeles, CA 90040 Wasabi outer package UPC 0 11152 29507 7 Ingredients: Wasabi: Seaweed, corn oil, sesame oil, wasabi powder (mustard {Ally Isothiocyante, Maltodextrin, arabic gum, palm oil, rosemary oleoresini}, dextrin, wasabi, FD&C Yellow #5, FD&C Blue No 1. Ingredients Original: Seaweed, Corn oil, Sesame oil, Salt.J F C International IncWasabi Flavor Seaweed snack is incorrectly packaged in Original Seaweed Flavor package which does not declare FD&C Yellow 5 and FD&C Blue No 1.Class II
2020-12-09YAGUMO AMANATTO GIFT BOX 6P 6/19.01 OZ JAN Code: 49 03089 39050 4 Imported by JFC International Inc. Los Angeles, CA 90040J F C International IncAma Natto (Sugar coated sweet beans) imported from Japan contains mold or the product may develop mold prior the best before date.Class II
2020-08-05Kasugai brand Matcha Ame (Green tea candy); 4.58 oz. plastic bag; 2 x 12 individual items per case Product of Japan Ingredients: glucose syrup, sugar, green tea powder, palm oil, artificial flavor. The label should include "mold lubricant oil (palm, rapseed, soybeans) Distributed by JFC International Inc. Los Angeles, CA UPC: 4 901326 035102J F C International IncUndeclared soybean which is contained in lubricant in candy mold.Class II
2018-02-14Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported by JFC International Inc., Los Angeles, CA.J F C International IncDaisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.Class I
2017-07-26Futaba Sesame Hijiki Rice Seasoning; 2.29 oz. glass jar; 4 902533 023173J F C International IncFirm discovered that seasoning product imported from Japan lacks an English language label and does not declare Wheat, Soybean and Fish (Bonito) allergens.Class I
2016-12-21You-ka Fresh Ramune Net Wt. 3.87oz (110g), Item No. 23925, 20 packs/caseJ F C International IncJFC International is recalling Fizzy Candy Punch Ramune because it may contain undeclared wheat allergen.Class II
2016-12-21You-ka Punch Ramune Net Wt. 3.87oz (110g), Item No. 23926, 20 packs/caseJ F C International IncJFC International is recalling Fizzy Candy Punch Ramune because it may contain undeclared wheat allergen.Class II
2014-10-29Hapi Pudding, 3-pack, net wt. 8.46oz, UPC 11152 13417, JFC item #13417J F C International IncProduct's label fails to declare milk.Class I

All 19 records for J F C International Inc

All 2013 recalls · All FDA food recall data

21 CFR 117.93 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.