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FDA food · drug · device recalls, merged

Before you eat it, take it, or plug it in — check.

Big Nope pulls three separate FDA recall feeds into one list per state, so you’re not searching three government databases to get one answer.

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced September 4, 2026

Foods AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusE. coliAnnounced September 3, 2026

Great ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc.Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenMilkUndeclaredAnnounced August 31, 2026

Little TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced August 29, 2026

Everything SproutsRobust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced August 29, 2026

MartinaMangoes

Potential contamination with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)

Recalls nationwide

Data last updated: September 10, 2026 at 1:16 PM UTC

19,422 recalls found
Wording
Class IIModerate risk
DrugRecalled June 13, 2023

Dry Eye Relief Lubricant Eye Drops, (Glycerin 0.2%, Hypromellose 0.2 %, Polyethylene glycol 400 1%), 0.5 FL OZ (15mL) bottle, packaged in a) equate, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716, 2-0.5 FL OZ (15 mL) Bottles, 1 FL OZ (30 mL) TOTAL, UPC 6 81131 36701 1, NDC 49035-280-02; b) DG health, DISTRIBUTED BY OLD EAST MAIN CO., 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072, UPC 0 95072 02656 0; c) sunmark, Distributed By McKesson, 6555 State Highway 161, Irving, TX 75039, UPC 0 10939 62144 3, NDC 49348-037-29; d) TopCare health, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007, UPC 0 36800 36100 3; e) HealthMart, Distributed by McKesson, 6555 State Highway 161, Irving, TX 75039, UPC 0 52569 13715 4; f) exchange select Artificial Tears, Manufactured for your Military Exchanges by: KC Pharmaceuticals, Inc., Pomona, CA 91768, UPC 6 14299 05620 6; g) meijer, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544, UPC 7 13733 29692 2, NDC 41250-718-01; h) H.E.B, MADE WITH PRIDE AND CARE FOR H.E.B, SAN ANTONIO, TX 78204, UPC 0 41220 43741 2; i) GeriCare, Distributed by: Gericare Pharmaceuticals Corp., 1650 63rd St., Brooklyn, NY 11204, UPC 3 57896 18405 6, NDC 57896-181-05

CGMP Deviations: good manufacturing deficiencies related to a lack of documentation of the fill line.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0898-2023
Lot/product code:
Lot #: a) LT21FO2, LT21F03, Exp 6/2023; b) LT21FO2, LT21F03, Exp 6/2023; c) LT21FO2, LT21F03, Exp 6/2023; d) LT21FO2, LT21F03, Exp 6/2023; e) LT21F02, Exp 6/2023; f) LT21F02, Exp 6/2023; g) LT21F03, Exp 6/2023; h) LT21F03, Exp 6/2023; i) LT21F03, Exp 6/2023
Recalling firm:
K.C. Pharmaceuticals, Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 21, 2023

Tizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Srikakulam - 532 409 India. NDC 55111-180-10

Failed dissolution specification: not meeting quality requirements results observed in 24-month long term stability testing.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0923-2023
Lot/product code:
Lot: T2100585, T2100586, T2100587, Exp 12/2023
Recalling firm:
Dr Reddy's Laboratories Limited
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 22, 2023

Diclofenac Sodium Topical Solution USP, 2% w/w, 3.8 FL.OZ.(112 grams) bottles, Rx only, Manufactured for: Alembic Pharmaceuticals, Inc. Bedminster, NJ 07921, USA Manufactured by: Alembic Pharmaceuticals Limited (Derma Division) Karakhadi, Vadodara 391450, India. NDC 62332-487-12

Defective Delivery System

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0941-2023
Lot/product code:
Lot #: 220151, 220152, 220153, Exp. Date 11/2024
Recalling firm:
ALEMBIC PHARMACEUTICALS, INC.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 26, 2023

Tizanidine Hydrochloride Tablet 4mg, packaged in a) 20 count-bottles (NDC 68788-7781-2), b)30-count bottles (NDC: 68788-7781-3), c) 60-count bottles, (NDC: 68788-7781-6), d) 90-count bottles (NDC: 68788-7781-9), e) 120-count bottles (NDC: 68788-7781-8), Rx only, Mfg: Dr. Reddy's Laboratories Limited.

Failed Stability Specifications

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0894-2023
Lot/product code:
Lot#: a) H1621S, Exp: 12/31/2023; b) H2321C, Exp: 12/31/2023; c) H0421B, Exp: 12/31/2023; d) H1721E, H1921T, H3121M, Exp: 12/31/2023, e) H2021G, Exp: 12/31/2023
Recalling firm:
Preferred Pharmaceuticals, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 10, 2023

Big Machine Distillery Hand Sanitizer Non-Sterile Solution Alcohol Antiseptic 80% Topical Solution, Produced and Distributed by Big Machine Distillery 1800 Abernathy Road Lynnville, TN 38472 a) 50 mL UPC 8 59105 00452 5; b) 100 mL UPC 8 59105 00453 2; c) 375 mL; d) 1/2 gallon; e) 1 gallon; f) 5 gallon; g) 55 gallon; i) Indianapolis Motor Speedway 50 mL UPC 8 59105 00452 5; j) Indianapolis Motor Speedway 375 mL UPC 8 59105 00454 9; k) Indianapolis Motor Speedway 1 gallon UPC 8 59105 00451 7; l) The Contributor 50 mL; m) Tony Kanaan Last Lap 100 mL; n) Tony Kanaan Last Lap 375 mL; o) Trexis Insurance 50 mL; p) Team Penske 50 mL; q) Middle Tennessee State University Lightning 50 mL.

CGMP Deviation: impurities exceed allowable limits.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0915-2023
Lot/product code:
All lots remaining within expiry.
Recalling firm:
Tenn South Distillery LLC dba Big Machine Distillery
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 11, 2023

Oxacillin for Injection, USP, 10 gram per pharmacy Bulk Package bottle, For Intravenous Use, Rx only, packaged as a) NDC 25021-163-99 and b) novaplus NDC 25021-163-68, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India.

Not guaranteed to be germ-free

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0937-2023
Lot/product code:
Lot: a) OXT202, exp 5/31/2025; OXT203, exp 5/31/2025; OXT301, exp 12/31/2025; b) OXT205, exp 6/30/2025; OXT204, exp 5/31/2025
Recalling firm:
Sagent Pharmaceuticals
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 11, 2023

Fingolimod Capsules, 0.5 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-476-30.

Failed Dissolution Specifications

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0925-2023
Lot/product code:
Lot 22122841, Exp August 2025
Recalling firm:
Ascend Laboratories, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 11, 2023

Oxacillin for Injection, USP, 1 gram per vial, For IV or IM Use, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India. NDC 25021-146-10.

Not guaranteed to be germ-free

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0935-2023
Lot/product code:
Lot: OXG301, Exp 12/31/2025
Recalling firm:
Sagent Pharmaceuticals
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 11, 2023

Oxacillin for Injection, USP, 2 grams per vial, For IV or IM Use, Rx only, labeled as a) NDC 25021-162-24 and b) novaplus NDC 25021-162-68, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. Made in India.

Not guaranteed to be germ-free

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0936-2023
Lot/product code:
Lot #: a) OXL202, exp 6/30/2025; OXL204, exp 6/30/2025; OXL301, exp 12/31/2025; OXL205, exp 11/30/2025; b) OXL201, exp 5/31/2025; OXL203, exp 6/30/2025
Recalling firm:
Sagent Pharmaceuticals
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusE. coliRecalled July 13, 2023

Food Research International - Uro Kid Support Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case

Potential contamination with E coli

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-1442-2023
Lot/product code:
Item # B6517 Lot #9237 Product # DRR6517-90VC Best By 01/26
Recalling firm:
Global Vitality Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 13, 2023

Testosterone Cypionate-Testosterone Propionate 180-20 mg/mL in cottonseed oil, Compounded Rx, For Intramuscular Use Only, a) 1 mL, b) 5 mL Multi-Dose Vial, New Vitalis Pharmacy, 4139 Cadillac Ct, Ste 201, Louisville, KY 40213

Not guaranteed to be germ-free

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0944-2023
Lot/product code:
Lot #: AL-05222023@901, BUD 7/22/23; AL-06122023@908CS, BUD 8/11/23
Recalling firm:
New Vitalis Pharmacy LLC dba New Vitalis Pharmacy
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusE. coliRecalled July 13, 2023

Food Research International - Serious Brain Enhancer Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case

Potential contamination with E coli

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-1443-2023
Lot/product code:
Item # B6506 Lot #9231 Product # DRR6506-90VC Best By 10/25
Recalling firm:
Global Vitality Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 21, 2023

Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Ampules per carton, Rx Only, For Oral Use Only - Not For Inhalation or Injection, Must be Diluted, Manufactured by: The Ritedose Corporation Columbia, SC 29203 for Ritedose Pharmaceuticals, LLC Columbia, SC 29203, NDC 76204-025-96.

CGMP deviation: product released prior to supplier approval.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0946-2023
Lot/product code:
Lot: 23CE2, Exp. 03/31/2026
Recalling firm:
The Ritedose Corporation
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenSoyUndeclaredRecalled July 27, 2023

BAPS SHAYONA Kopra Paak Coconut fudge Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53119 Contains: Milk

During an FDA inspection the firm was notified that some of their products contains not listed on the label soy.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0492-2024
Lot/product code:
A06D2023 BEST BY 7/19/2023
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodUndeclaredRecalled July 27, 2023

BAPS SHAYONA Kaju Pista Roll Sweet rolls made from cashew and pistachio filling Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53068 Contains: Nuts

During an FDA inspection the firm was notified that some of their products contains not listed on the label Yellow #5 & #6 and Blue 1.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0490-2024
Lot/product code:
02F1823 BEST BY 8/2/23
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenSoyUndeclaredRecalled July 27, 2023

BAPS SHAYONA Burfi Sweetened ricotta fudge Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53037 Contains: Milk

During an FDA inspection the firm was notified that some of their products contains not listed on the label soy.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0496-2024
Lot/product code:
A03E2123 Best By 7/20/2023, A03E2023 Best By 7/19/2023 & A02E0423 Best By 7/3/2023
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodUndeclaredRecalled July 27, 2023

BAPS SHAYONA Motichur Ladoo Sweet chickpea flour mini-pearls rolled into spheres Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53160 Contains: Milk

During an FDA inspection the firm was notified that some of their products contains not listed on the label Yellow #5 & #6.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0494-2024
Lot/product code:
02G0623 BEST BY 08/20/2023, 02G0623 BEST BY 8/20/2023, BEST BY 08/15/2023, 04F1423 BEST BY 7/29/2023 & 11F0823 BEST BY 7/23/2023
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodUndeclaredRecalled July 27, 2023

BAPS SHAYONA Anjir Roll Sweet rolls made from fig and nut filling Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53005 Contains: Milk, Nuts

During an FDA inspection the firm was notified that some of their products contains not listed on the label Yellow #5.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0485-2024
Lot/product code:
03 G2023, BEST BY 9/18/23 & 01 F1923, BEST BY 8/18/23
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenSoyUndeclaredRecalled July 27, 2023

BAPS SHAYONA Kesar Penda Ricotta fudge discs flavored with saffron Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53150 Contains: Milk

During an FDA inspection the firm was notified that some of their products contains not listed on the label soy and Yellow #5 & #6.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0491-2024
Lot/product code:
11G1323 BEST BY 9/11/2023, 04G0523 BEST BY 9/3/2023, 04F1523 BEST BY 8/14/2023, 04F0723 BEST BY 8/6/2023 & 04F0723 BEST BY 8/6/2023
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodUndeclaredRecalled July 27, 2023

BAPS SHAYONA Kaju Katri Kesar Cashew fudge flavored with saffron Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53065 Contains: Nut

During an FDA inspection the firm was notified that some of their products contains not listed on the label Yellow #5.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0489-2024
Lot/product code:
10G1323 BEST BY 08/26/23
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodUndeclaredRecalled July 27, 2023

BAPS SHAYONA Bundi Ladoo Sweet chickpea flour pearls rolled into spheres Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53094 Contains: Milk, Nuts

During an FDA inspection the firm was notified that some of their products contains not listed on the label Yellow #5, Red 40 & 3 and Green 3.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0487-2024
Lot/product code:
02G1223, BEST BY 08/26/23, 01 F1823 BEST BY 8/2/23, 01 F0723 BEST BY 07/22/2023, 02F0123 BEST BY 7/16/2023
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodUndeclaredRecalled July 27, 2023

BAPS SHAYONA Badam Pista Sandwich Almond and pistachio layered fudge Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53009 Contains: Nuts

During an FDA inspection the firm was notified that some of their products contains not listed on the label Yellow #5, Green 3.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0486-2024
Lot/product code:
03G1723, BEST BY 9/15/23
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenSoyUndeclaredRecalled July 27, 2023

BAPS SHAYONA Surti Ghari Sweet dumplings stuffed with minced nuts and glazed with clarified butter Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53102 Contains: Milk

During an FDA inspection the firm was notified that some of their products contains not listed on the label soy and Yellow #6.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0495-2024
Lot/product code:
A07E2923 Best By 7/28/2023
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenSoyUndeclaredRecalled July 27, 2023

BAPS SHAYONA Mohanthal Fudge-like sweet made with chickpea flour roasted in clarified butter Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53126 Contains: Milk, Nuts

During an FDA inspection the firm was notified that some of their products contains not listed on the label soy, Yellow #5 & #6.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0493-2024
Lot/product code:
A02G2423 Best By 9/22/2023 & A04E2423 Best By 7/23/2023
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenSoyUndeclaredRecalled July 27, 2023

BAPS SHAYONA Sangam Katri Rose and nut fudge Net Wt: 12 Oz 460 Rockbridge Rd NW Lilburn, GA 30047 UPC 53035 Contains: Nuts

During an FDA inspection the firm was notified that some of their products contains not listed on the label soy.

Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-0497-2024
Lot/product code:
04G1723 BEST BY 9/15/2023 & 03F0523 BEST BY 8/4/2023
Recalling firm:
BAPS Shayona
View official FDA record (opens in a new tab)