NY Establishment Recalls Pasta Product After Formulation Changes Adds Undeclared Egg

Whitson’s Food Service (Bronx) Corp., an Islandia, N.Y., establishment, is recalling approximately 8,713 pounds of frozen, ready-to-cook chicken alfredo with broccoli and penne pasta meals due to misbranding and undeclared allergens, in this case, the product contains egg, a known allergen, which is not declared on the product label.  The problem was discovered when the producing establishment received a consumer complaint and notified FSIS. The establishment investigated and determined that they updated the product formulation with a sauce containing egg, but the information was not provided to the nutrition department that creates the product labels. As a result, the immediate product labels do not list egg as an allergen and the case labels do not list egg in the ingredient statement.

https://www.fsis.usda.gov/recalls-alerts/whitsons-food-service-bronx-corp--recalls-frozen-ready-cook-chicken-alfredo-broccoli
Whitson’s Food Service (Bronx) Corp. Recalls Frozen, Ready-To-Cook Chicken Alfredo with Broccoli and Penne Pasta Products Due to Misbranding and Undeclared Allergens.

Food Importers Cited for Not Having FSVP - Jan-Feb 2023 Edition

FDA issued Warning Letter to the following food importers for not having a FSVP in place for their imported foods.

Sohgave LLC of Houston, TX did not develop, maintain, and follow an FSVP for any imported foods including Honey from one foreign company and Agave Syrup, honey, coconut syrup and inulin syrup imported from another.
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/sohgave-llc-646874-01192023

AMO and Wing Inc. dba T and H Trading Co. of Oakland, CA - as "a very small importer is must obtain written assurance, in accordance with 21 CFR 1.512(b)(3), before importing the food and at least every two years thereafter, that your foreign supplier is producing the food in compliance with processes and procedures that provide at least the same level of public health protection as those required under section 418 or 419 of the FD&C Act, if either is applicable, and the implementing regulations, and is producing the food in compliance with sections 402 and 403(w) (if applicable) of the FD&C Act. Specifically, you did not provide written assurances from your foreign suppliers for any of the foods you import, including dried noodle and dried bean curd from (b)(4); and vermicelli from (b)(4)."
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/amo-and-wing-inc-dba-t-and-h-trading-co-638293-12072022

HST Produce, Inc. of Houston, TXdid not develop, maintain, and follow an FSVP as required by section 805 of the FD&C Act and 21 CFR part 1.502(a). Specifically, the firm did not develop, maintain, and follow an FSVP for any of their imported foods including each of the following foods:
Fresh prickly pear imported from (b)(4), Fresh jalapeno pepper imported from (b)(4), Peruano beans imported from (b)(4)
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/hst-produce-inc-639794-11072022

S&S Quality Wholesale Inc. of El Cajon, CA did not develop, maintain, and follow an FSVP as required by section 805 of the FD&C Act and 21 CFR part 1.502(a). for any of thier imported foods including:  Bashan Koftelik Bulgur Fine imported from (b)(4), located in (b)(4), Bread Sticks imported from (b)(4), located in (b)(4),Wheat Kernal Habiya imported from (b)(4), located in (b)(4)
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/ss-quality-wholesale-inc-630772-06012022

Leimax, Corp of Yonkers, NY did not develop an FSVP for any of the their imported foods including each of the following foods: Lollipops ((b)(4)) manufactured by (b)(4). Cola flavored soft drink manufactured by (b)(4). (b)(4) hot sauce manufactured by (b)(4).
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/leimax-corp-633364-10072022

Fuentes Farms LLC of McAllen, TX 7 did not develop, maintain, and follow an FSVP as required by section 805 of the FD&C Act and 21 CFR 1.502(a).for any of their imported foods including: green onions imported from foreign supplier (b)(4) chayote imported from foreign supplier (b)(4)
broccoli imported from foreign supplier (b)(4)

"You import fresh produce, that is “covered produce” as defined in 21 CFR 112.3. As an importer of covered produce, you must have an FSVP that demonstrates that your supplier is producing the food in compliance with processes and procedures that provide at least the same level of public health protection as those required under section 419 of the FD&C Act (21 U.S.C. § 350h) (regarding standards for produce safety) and the implementing regulations in the Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption (21 CFR part 112)."
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/fuentes-farms-llc-642138-10142022

TL State Management of Brooklyn, NY did not develop an FSVP for any of their imported  food products including Pickled red tomatoes from (b)(4)  Puff pastry dough from (b)(4) and (b)(4) wafers from (b)(4)
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/tl-state-management-inc-634663-08302022

San-Rey Produce Inc.of Pharr, Texas. did not develop an FSVP for any of their imported foods including:  onions imported from foreign supplier, (b)(4), (b)(4) limes imported from foreign supplier, (b)(4) and coriander imported from foreign supplier,
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/san-rey-produce-inc-643593-12072022

FDA Issues a Warning Letter to Processor of Aseptic Nutritional Beverages for Inadequate Handling of Process Deviations

FDA issued a Warning Letter to Lyons Magnus, a CA company with a Wisconsin based processing operation for aseptically packaged nutritional beverages. The inspection was conducted in response to a recall that occurred in July of 2022 due to an under-processing issue of the low acid product that had the potential to allow pathogens such as Clostridium botulinum survive.

The issue that caused the recall was when the company identified gram positive rods in the product....but this was not the first time the company found organisms in the finished product. FDA states "Your notification to FDA occurred (b)(4) after your positive lab tests for gram-positive rods on (b)(4), and (b)(4) after lab testing confirmed the Bacillus subtilis result. Moreover, our review of your micro testing records dating back to (b)(4), noted your internal microbiological tests indicated gram-positive, gram-negative rods, and cocci in approximately 37 batches of finished products which were released and shipped. These test results demonstrate the presence of viable microorganisms in your commercial products, the majority of which you had not previously reported to FDA. "

FDA goes on to state, "We remind you that your aseptically packaged products containing viable microorganisms do not meet the definition of commercial sterility, per 21 CFR 113.3(e)(1)(i)(a) and are, therefore, adulterated. Shipping adulterated products into interstate commerce is a prohibited act under section 301(a) of the Act. Under 21 CFR 108.35(e) your firm must promptly alert FDA of lots shipped with known microbial contamination, not just those lots with confirmed species as identified in July 2022. Additionally, you shipped these products without conducting a full investigation into the cause of the microbial contamination. You indicated in your October 5, 2022, response that micro findings prior to April 2022 were attributed to laboratory error, yet you did not conduct an assessment of your laboratory practices prior to April 2022. Microbial findings in finished product indicate a loss of sterility during production of that batch and warrant further investigation. Per 21 CFR 113.40(g)(2)(ii)(B), “[i]n the event of loss of sterility, the system(s) shall be returned to a condition of commercial sterility before resuming packaging operations.”

It seems that much of the issue resulted when the company completed a process change that increased the volume run through the processor.  And although the company recognized a microbial contamination issue, they continued to run the modified process.  There were also indicators with the cleaning process was not effective.  There were some additional comments regarding their handling of process deviations.

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/lyons-magnus-llc-645766-01302023

WARNING LETTER
Lyons Magnus, LLC

MARCS-CMS 645766 — JANUARY 30, 2023
Recipient:
Edward Carolan
Chief Executive OfficerLyons Magnus, LLC

FDA Issues Warning Letter to Cruise Line for Not Maintaining Safe Water Supply

FDA inspected American Cruise Line's American Star and American Heritage vessels from in April 2022, through June 2022, and from June 2022, through August 2022. The investigation and inspections were initiated by FDA after three passengers who traveled in April 2021, September 2021, and September-October 2021 aboard these vessels were diagnosed with Legionnaires’ disease. FDA investigators collected biofilm swabs and potable water samples from these vessels and identified Legionella pneumophilia serogroup 1 and Legionella spp. in the potable water system of the vessels thus determine that the water is adulterated as defined by regulation..

FDA had issues with the response by the company in terms of response to the issue. There were issues with the test methodology the company was using..The company did "not monitor potable water parameters, such as free or total chlorine residual, temperature, and pH on the vessel when docked and not in operation or while in operation."

ProSobee Simply Plant-Based Infant Formula Due to Possibility of Cross-contamination with Cronobacter sakazakii

Reckitt, a producer of nutrition products, announced today that, out of an abundance of caution, it has chosen to voluntarily recall two (2) select batches of ProSobee 12.9 oz. Simply Plant-Based Infant Formula due to a possibility of cross-contamination with Cronobacter sakazakii. All product distributed went through extensive testing and tested negative for the bacteria.
 

According to the report, "The batches in question tested negative for Cronobacter and other bacteria and this is an isolated situation. After a thorough investigation, we have identified the root cause, which was linked to a material from a third party. We have taken all appropriate corrective actions, including no longer sourcing this material from the supplier."


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/reckitt-recalls-two-batches-prosobee-129-oz-simply-plant-based-infant-formula-because-possible
Reckitt Recalls Two Batches of Prosobee 12.9 oz Simply Plant Based Infant Formula Because of Possible Health Risk
Summary
Company Announcement Date:  February 20, 2023
FDA Publish Date:  February 20, 2023
Product Type:  Food & Beverages  Infant Formula & Foods
Reason for Announcement:   Potential Cronobacter sakazakii contamination
Company Name:  Reckitt
Brand Name:  Enfamil ProSobee
Product Description:  Enfamil Prosobee Simply Plant-Based Infant Formula in 12.9 oz containers

More Enoki Mushrooms Recalled for Listeria After MD State Lab Finds Positive Sample

Xin Ao International Group Corp of Linden, NJ, is recalling its 200 grams packages of “Sss Enoki Mushroom” and “K-Fresh Mushroom”, because it has the potential to be contaminated with Listeria monocytogenes.  The recall was the result of a routine sampling program by Maryland Department of Health which revealed that the finished products contained the bacteria. The company has ceased the production and distribution of the product as FDA and the company continue their investigation as to what caused the problem.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/xin-ao-international-group-corp-recalls-sss-enoki-mushroom-k-fresh-mushroom-because-potential-health
Xin Ao International Group Corp. Recalls "Sss Enoki Mushroom" & “K-Fresh Mushroom” Because of Potential Health Risk
Summary
Company Announcement Date:  February 17, 2023
FDA Publish Date:  February 17, 2023
Product Type:  Food & Beverages
Reason for Announcement:  Listeria monocytogenes
Company Name:  Xin Ao International Group Corp.
Brand Name:  Xin Ao International Group Corp.
Product Description:  Enoki Mushrooms

Valentine Candy Recalled for Undeclared Tree Nuts

Silvestri Sweets Inc. of Geneva, IL is voluntarily recalling its 8 ounce bags of Favorite Day branded Valentine’s Milk Chocolate Covered Caramels with Nonpareils because they may contain an undeclared tree nut.   The recall was initiated after it was discovered that possible tree nut inclusions were distributed in packaging and/or product that did not reveal the presence of tree nuts. Subsequent investigation indicates the problem may have been caused by a temporary breakdown in the company’s production and packaging process.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/silvestri-sweets-issues-voluntary-allergy-alert-undeclared-pecan-milk-chocolate-caramels
Silvestri Sweets Issues Voluntary Allergy Alert on Undeclared Pecan in Milk Chocolate Caramels
Summary
Company Announcement Date: February 14, 2023
FDA Publish Date:  February 16, 2023
Product Type:  Food & Beverages  Snack Food Item  
Reason for Announcement:  Undeclared pecan allergen
Company Name:  Silvestri Sweets Inc.
Brand Name:  Favorite Day
Product Description:  Milk Chocolate Covered Caramels with Nonpareils

Asian Spice Mix Recalled for Undeclared Sesame After Mislabeling Incident

Wismettac Asian Foods, Inc., Santa Fe Springs, CA is recalling 10.58 oz packages of Shirakiku brand Spice Seasoning products (Spice Ichimi Togarashi 300g and Spice Shichimi Togarashi 300g). The product package of Ichimi spice seasoning contains Shichimi spice seasoning contents (incorrect package) causing the undeclared allergen of sesame seeds. The outer carton of “Ichimi” and “Shichimi” may possibly contains inner packages of “Ichimi”, and the inner packages contain “Shichimi” contents. The recall was initiated after it was discovered that the product containing sesame was distributed in packaging that did not reveal the presence of sesame. Subsequent investigation indicates the problem was caused by a human error during the packing process.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wismettac-asian-foods-issues-allergy-alert-undeclared-spice-seasoning
Wismettac Asian Foods Issues Allergy Alert on Undeclared Spice Seasoning
Summary
Company Announcement Date:  February 14, 2023
FDA Publish Date:  February 14, 2023
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared sesame
Company Name:  Wismettac Asian Foods, Inc.
Brand Name:  Shirakiku
Product Description:  Ichimi spice powder, 10.58 oz

CA Distributor Pulls More Imported Snack Products for Lack of Allergen Labeling

Daiso California LLC of La Mirada, CA is recalling even more snack products that lack proper allergen labeling.  This company has issued other recalls over the past few months for the same issue....lack of allergen labeling on imported snack products.  The last posted recall was issue on February 3, 2023.


https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/daiso-issues-allergy-alert-prepackaged-snacks-0
Daiso Issues Allergy Alert for Prepackaged Snacks
Summary
Company Announcement Date: February 13, 2023
FDA Publish Date:  February 13, 2023
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared milk, wheat, soy, tree nuts
Company Name:  Daiso California, LLC
Brand Name:  Various
Product Description:   Various Snack Foods