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Recalls affecting Texas

Data last updated: September 7, 2026 at 12:15 AM UTC

17,378 recalls found

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/virusAnnounced 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/virusAnnounced 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)
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)
UnclassifiedAllergenUndeclaredAnnounced 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)
UnclassifiedBacteria/virusAnnounced 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/virusAnnounced 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)
Wording
Class IHigh risk
DrugRecalled November 13, 2023

Target brand High Performance Lubricant Eye Drops (Polyethylene glycol 400 0.4%, Propylene glycol 0.3%) a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 11673-522-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 11673-522-30), Distributed by: Target Corporation Minneapolis, MN 55403

Non-Sterility

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0300-2024
Lot/product code:
All lots
Recalling firm:
Kilitch Healthcare India Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 13, 2023

Leader brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%), packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 70000-0090-1) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 70000-0090-2), Distributed by: Cardinal Health Dublin, Ohio 43017

Non-Sterility

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0291-2024
Lot/product code:
All lots
Recalling firm:
Kilitch Healthcare India Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 13, 2023

Multi-action Relief Drops (Polyvinyl alcohol 0.5%, Providone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-2254-3

Non-Sterility

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0308-2024
Lot/product code:
All lots
Recalling firm:
Kilitch Healthcare India Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 13, 2023

LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%), packaged 0.5 FL OZ (15mL) bottles (Twin Pack), Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4811-5

Non-Sterility

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0304-2024
Lot/product code:
All lots
Recalling firm:
Kilitch Healthcare India Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 17, 2023

Vigabatrin for Oral Solution, USP 500 mg per packet, 50 packets per box, Rx Only, Manufactured by: InvaGen Pharmaceuticals, Inc., (a subsidiary of Cipla Ltd.), Hauppauge, NY, 11788, Manufactured for: Cipla USA, Inc., Warren, NJ 07059, NDC 69097-964-53

Defective Container: powder may leak out of the pouch

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0220-2024
Lot/product code:
Lot #: NB301030, Exp. Date 03/31/2025
Recalling firm:
InvaGen Pharmaceuticals, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled November 22, 2023

TING 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder, NET WT 4.5 oz (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591, UPC 363736532611.

Chemical Contamination; presence of benzene.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0151-2024
Lot/product code:
Lot #s: 0H88645, Exp 07/31/2024; 0B88345, Exp 02/29/2024.
Recalling firm:
Insight Pharmaceuticals Corporation
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 22, 2023

SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936. NDC 0078-0110-22

Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0144-2024
Lot/product code:
Lot #: FX001500, FX001582, Exp. 09/30/2024
Recalling firm:
Novartis Pharmaceuticals Corporation
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled November 29, 2023

Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack, Distributed by Magnum Los Angelas CA. UPC 6 45759 99300 7. Amazon's ASIN# B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ

Marketed without an approved NDA/ANDA: Magnum XXL found to contain not listed on the label active pharmaceutical ingredient (API) - Sildenafil.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0206-2024
Lot/product code:
All Lots
Recalling firm:
Meta Herbal
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 21, 2023

8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 50 mL Syringe per Carton, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-6637-24 (carton), 0409-6637-14 (case).

Presence of Particulate Matter; identified as glass

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0234-2024
Lot/product code:
Lot HA7295, EXP 03/01/2025
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 21, 2023

4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake Forst, IL 60045, NDC 0409-5534-24 (carton), 0409-5534-14 (case).

Presence of Particulate Matter; identified as glass

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0233-2024
Lot/product code:
Lot GX1542, Exp. 01/01/2025
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled December 21, 2023

Americaine, (benzocaine 20%) Benzocaine Topical Anesthetic Spray, Aerosol Can 2 oz (57 G), Dist. by Insight Pharmaceuticals Corp. Tarrytown, NY 10591, USA, A Prestige Consumer Healthcare company. Made in India. NDC 63736-378-02, Can UPC 3 63736 37882 0; Case UPC 1 03 63736 37882 7

Chemical Contamination: presence of benzene

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0236-2024
Lot/product code:
Lot # 1A16420, exp. date 01/31/2025
Recalling firm:
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 21, 2023

Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake FOrest, IL 60045, NDC 0409-4911-11 (carton), 0409-4911-34 (case).

Presence of Particulate Matter; identified as glass

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0235-2024
Lot/product code:
Lot GY2496, Exp 02/01/2025
Recalling firm:
Pfizer Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 21, 2023

Bleomycin for Injection, USP, 15 units per vial, 1 single dose glass fliptop vial, Rx Only, Distributed by: Hospira, Inc., Lake Forest, IL 68045, NDC 61703-332-18

Presence of particulate matter: glass

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0261-2024
Lot/product code:
Lot #: BL12206A, Exp date 06/30/2024
Recalling firm:
PFIZER
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 26, 2023

Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg, Dextromethorphan HBr 20 mg), a) 4 FL OZ (118mL) and b) 8 FL OZ (237 mL) bottles, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059

Microbial Contamination of Non-Sterile Products

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0316-2024
Lot/product code:
a) Lot#: T10810, Exp 10/31/2025 b) Lot#: T08730, T08731, T08732, T08733, Exp 05/31/2025; T10808, Exp 09/30/2025
Recalling firm:
Haleon US Holdings LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 26, 2023

Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg, Diphenhydramine HCl 25mg), 8 FL OZ (237 mL) bottle, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059

Microbial Contamination of Non-Sterile Products

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0317-2024
Lot/product code:
Lot#: T08740, T08742, Exp 06/30/2026
Recalling firm:
Haleon US Holdings LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride (80 mcg per mL), Item F3360, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-148-94.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0279-2024
Lot/product code:
Lot #: 2330993, Exp. Date 02/15/2024; 2331010, Exp. Date 02/10/2024; 2331055, Exp. Date 01/18/2024; 2331113, Exp. Date 02/26/2024; 2331181, Exp. Date 03/04/2024; 2331187, Exp. Date 03/23/2024; 2331266, Exp. Date 03/31/2024; 2331343, Exp. Date 04/01/2024; 2331349, Exp. Date 04/23/2024; 2331433, Exp. Date 05/05/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

FentaNYL citrate PF, 2500 mcg per 250 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3342, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-072-82.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0278-2024
Lot/product code:
Lot #: 2330988, Exp. Date 01/31/2024; 2331058, Exp. Date 02/18/2024; 2331150, Exp. Date 03/10/2024; 2331231, Exp. Date 03/24/2024; 2331289, Exp. Date 03/30/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

FentaNYL citrate PF, 1000 mcg per 100 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3355, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-072-41.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0277-2024
Lot/product code:
Lot #: 2331062, Exp. Date: 02/08/2024; 2331224, Exp. Date 03/18/2024; 2331270, Exp. Date 03/28/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

PHENYLephrine HCl 40 mg per 250 mL 0.9% Sodium Chloride (160 mcg per mL), Item F3352, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-150-82.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0280-2024
Lot/product code:
Lot #: 2330939, Exp. Date 01/30/2024; 2331032, Exp. Date 02/03/2024; 2331112, Exp. Date 03/19/2024; 2331190, Exp. Date 03/26/2024; 2331429, Exp. Date 04/28/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3206, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-028-68.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0281-2024
Lot/product code:
Lot #: 2331184, Exp. Date 02/13/2024; 2331185, Exp. Date 02/10/2024; 2331189, Exp. Date 02/20/2024; 2331191, Exp. Date 02/24/2024; 2331258,Exp. Date 03/03/2024; 2331317, Exp. Date 03/15/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled December 28, 2023

VANCOmycin HCl PF 1.5g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3208, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-029-68.

Stronger than it should be Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0282-2024
Lot/product code:
Lot #: 2331140, Exp. Date 02/08/2024; 2331188, Exp. Date 02/15/2024; 2331261, Exp. Date 03/05/2024; 2331287, Exp. Date 03/14/2024.
Recalling firm:
Denver Solutions, LLC DBA Leiters Health
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Monterey Jack Conventional (bulk)

Listeria monocytogenes contamination.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0928-2024
Lot/product code:
PLU Batch ID 40200 1DZ-23249 40200 2DY-23249 40200 3DX-23249 40200 4CW-23249 40200 1DY-23279 40200 2DX-23279 40200 3CW-23279 40200 4CZ-23279 40200 1DZ-23283 40200 2DY-23283 40200 3CW-23283 40200 4CZ-23283 40200 2EY-23284 40200 3EX-23284 40200 4EW-23284 40200 1EX-23314 40200 2DW-23314 40200 3DZ-23314 40200 4DY-23314 40200 1DZ-24019 40200 2EY-24019 40200 3EX-24019 40200 4EW-24019 40200 1CY-24027 40200 2DX-24027 40200 3DW-24027 40200 4DZ-24027
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Tio Francisco Queso Para Freir 16 oz. Tio Francisco Queso Para Freir Available to consumers at retail deli counters in various sizes Freir (bulk)

Listeria monocytogenes contamination.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0922-2024
Lot/product code:
All dates through 04/17/2024 Freir (bulk) PLU Batch ID 101 1EW-23312 101 1DY-23313 101 2EW-23319 101 2EW-23320 101 3EW-23325 101 3EY-23333 101 4EW-23334 101 1EX-23345 101 2DY-23354 101 1EX-23362 101 2EX-24004 101 4EW-24018 101 1EW-24026
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Rizo Bros Cotija (Grated) 8 oz. UPC 72724200043 7 oz. UPC 7-27242-14022-5 Tio Francisco, Casa Cardenas 9 oz. UPC 7-27242-00022-2 & 8-11371-27109-4 Rizo Bros Cotija 8 oz. UPC 7-27242-00043-7 Tio Francisco Cotija 14 oz. 7-27242-00517-3 Food City Cotija 16 oz. Tio Francisco Cotija (Grated) 20 oz. UPC 7-27242-00056-7 Tio Francisco, San Carlos Available to consumers at retail deli counters in various sizes Tio Francisco Cotija Enchilado 14 oz. UPC 7-27242-00535-7 Food City, Casa Cardenas Cotija Enchilado 16 oz. Tio Francisco Cotija Enchilado Available to consumers at retail deli counters in various sizes Tio Francisco Cotija Rallado 12 oz. UPC 7-27242-00021-5 Tio Francisco Cotija Rallado Available to consumers at retail deli counters in various sizes Cotija (Bulk and grated bulk)

Listeria monocytogenes contamination.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0916-2024
Lot/product code:
All dates through 07/31/2024 Bulk Products: PLU Batch ID 006 3FX-23219 031 1EZ-23219 42019 1EZ-23219 56010 2EY-23219 006 3FY-23220 001 4FX-23221 008 4FX-23221 019 1EW-23221 034 4FX-23221 019 1DX-23222 019 3EZ-23222 019 4EY-23222 019 2FX-23223 004 4FZ-23226 011 1EX-23226 019 3FY-23226 019 4FZ-23226 031 3FY-23226 004 3FX-23227 004 4EW-23227 56010 1EZ-23227 56010 2EY-23227 031 4FX-23228 045 1EW-23228 12006 4FX-23228 42019 4FX-23228 004 1EZ-23229 019 1EZ-23229 019 2EY-23229 019 4FW-23229 031 1EZ-23229 031 4FW-23229 56010 3EX-23229 004 1EZ-23233 004 4FW-23233 011 3EX-23233 001 1EY-23234 006 4EZ-23234 008 1EY-23234 034 1EY-23234 019 2EZ-23235 019 3EY-23235 019 4EX-23235 42019 2EZ-23235 006 3FY-23236 019 1EW-23236 019 2EZ-23236 019 4FX-23236 12006 4FX-23236 019 1EX-23237 019 2EZ-23237 004 1EW-23240 004 3FY-23240 004 4FX-23240 019 1EW-23240 031 1EW-23240 56010 2EZ-23240 019 1EY-23241 019 3FX-23241 019 4EW-23241 030 2EZ-23241 56002 1DZ-23241 56002 3EX-23241 56002 4DW-23241 019 3FY-23242 031 3FY-23242 034 1EW-23242 001 1EW-23243 004 3FZ-23243 006 2FX-23243 008 1EW-23243 019 1EW-23243 019 3FZ-23243 031 1EW-23243 032 1EW-23243 12006 1EW-23243 56010 4EY-23243 004 2FX-23248 006 3FW-23248 011 1EY-23248 019 4EZ-23248 004 4EW-23249 006 3FX-23249 031 1EZ-23249 031 4EW-23249 12006 1EZ-23249 56002 4DW-23249 56006 3FX-23249 019 2FX-23250 019 3FW-23250 031 2FX-23250 004 2EZ-23254 045 1EW-23254 046 3EX-23254 004 1EY-23255 004 2FW-23255 004 3EZ-23255 42019 1EY-23255 56010 4EX-23255 019 1EZ-23256 031 1EZ-23256 031 3EX-23256 42019 3EX-23256 006 1EW-23257 12006 1EW-23257 008 3EZ-23261 019 2EW-23261 019 3EZ-23261 032 1EX-23261 034 1EX-23261 56010 4EY-23261 006 1FX-23262 006 2EW-23262 011 4EY-23262 019 2FX-23263 019 3FW-23263 031 3FW-23263 031 4EZ-23263 42019 4EZ-23263 019 3FY-23264 12006 4FX-23264 019 2FY-23265 019 3FX-23265 030 1DZ-23265 031 3FX-23265 004 2EY-23268 004 3FW-23268 006 4EZ-23268 031 2EY-23268 031 3FW-23268 56001 2EY-23268 56006 4EZ-23268 56010 1EX-23268 004 1EW-23269 004 3EY-23269 006 4EX-23269 019 2FZ-23269 56010 2EZ-23269 019 3EX-23270 045 1EZ-23270 019 1EX-23271 019 2EZ-23271 42019 4FY-23271 0074 3FW-23275 019 1FY-23276 019 2EX-23276 56010 4EZ-23276 004 3EY-23277 006 1EW-23277 006 2EZ-23277 011 4EX-23277 019 3EY-23277 12006 2EZ-23277 004 3FY-23278 001 1EZ-23282 008 1EZ-23282 019 1EZ-23282 034 4EW-23282 56010 2EY-23282 006 1EW-23283 019 1EW-23283 019 4EY-23283 031 4EY-23283 12006 1EW-23283 006 4FX-23284 004 1EW-23285 004 2EZ-23285 004 3EY-23285 019 3EY-23285 006 3FW-23289 56010 2EX-23289 019 1FX-23290 019 2EW-23290 019 3EZ-23290 031 3EZ-23290 046 4EY-23290 004 3EX-23291 004 4EW-23291 006 2EY-23291 004 2EX-23292 006 4FZ-23292 019 3EW-23292 031 3EW-23292 12006 4FZ-23292 006 3FX-23296 019 2FY-23296 019 4EW-23296 12006 3FX-23296 42019 2FY-23296 56006 3FX-23296 56010 1EZ-23296 019 4FX-23297 045 1EW-23297 56010 3EY-23297 019 1FY-23298 019 2FZ-23298 019 1EZ-23299 019 2EY-23299 019 3EX-23299 002 2EW-23303 004 1EX-23303 019 2FW-23303 019 4EY-23303 004 1FY-23304 004 2EX-23304 006 3EW-23304 011 4EZ-23304 12006 1FY-23304 006 1EW-23305 008 3FZ-23305 019 2EZ-23305 019 3FZ-23305 019 4FY-23305 0074 2EZ-23306 019 1EW-23306 001 4EY-23310 019 4EY-23310 56010 1EW-23310 011 2EY-23311 019 1EZ-23311 019 3FX-23311 019 4EW-23311 006 1FX-23312 019 3EY-23312 031 1FX-23312 031 4EX-23312 12006 4EX-23312 42019 1FX-23312 42019 3EY-23312 004 1EY-23313 004 2EX-23313 004 3EW-23313 004 4EZ-23313 006 1EY-23313 12006 1EY-23313 56010 2EW-23314 019 1BZ-23317 019 2BY-23317 56010 4AW-23317 019 1FZ-23318 12006 1FZ-23318 004 1EX-23319 004 3FZ-23319 004 4EY-23319 019 2FX-23319 019 4EY-23319 006 3FZ-23320 019 4EY-23320 42019 3EX-23324 006 2EX-23325 019 1EY-23325 031 1EY-23325 031 4EZ-23325 045 3FX-23325 12006 2EX-23325 004 1FX-23331 004 3FZ-23331 004 4EY-23331 019 2FW-23331 019 4EY-23331 046 1EX-23331 006 3FX-23332 006 4EW-23332 56010 1EZ-23332 008 2EZ-23333 019 1FW-23333 031 1FW-23333 56006 2EZ-23333 0074 4FX-23334 019 1EZ-23334 019 2EY-23334 019 3EX-23334 031 3EX-23334 12006 4FX-23334 004 3FX-23335 019 3FX-23335 004 1FX-23338 006 3FZ-23338 019 1FX-23338 019 2FW-23338 031 1FX-23338 42019 2FW-23338 56010 4EY-23338 008 2FX-23339 031 2FX-23339 42019 2FX-23339 019 1FW-23340 032 3EY-23340 034 3EY-23340 56010 4EX-23340 006 3FZ-23345 019 4EY-23345 006 2FW-23348 019 3FZ-23348 011 3FW-23349 019 4FY-23349 56006 2FX-23349 004 1EW-23353 004 4EX-23353 0074 3FY-23353 019 4EX-23353 031 3FY-23353 031 4EX-23353 56010 2EZ-23353 004 1EZ-23354 019 3EX-23354 045 4EW-23354 011 2EY-23355 019 1EZ-23355 019 3FX-23355 045 4EW-23355 006 3FZ-23360 12006 3FZ-23360 56006 3FZ-23360 004 1DZ-23361 019 4EX-23361 56010 3EY-23361 004 2FW-23362 004 3FZ-23362 019 3FZ-23362 12006 4EY-23362 006 4EY-23363 019 2FW-23363 019 3FZ-23363 004 3FW-24002 011 1EY-24002 019 4EZ-24002 031 2FX-24002 031 4EZ-24002 42019 2FX-24002 004 4EW-24003 006 1EZ-24003 019 3EX-24003 56006 1EZ-24003 006 3FW-24005 56010 1EY-24005 001 1EW-24008 008 1EW-24008 019 1EW-24008 031 1EW-24008 032 4FX-24008 034 4FX-24008 56010 2EZ-2400… (truncated, 9613 characters total — see the official FDA record for the full value)
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Rizo Bros. Oaxaca 8 oz. UPC 7-27242-00334-6 Tio Francisco Oaxaca 12 oz. UPC 7-27242-12332-7 Tio Francisco Oaxaca 14 oz. UPC 7-27242-00532-6 Food City Oaxaca 16 oz. Tio Francisco, San Carlos Available to consumers at retail deli counters in various sizes Tio Francisco Oaxaca (shred) Available to consumers at retail deli counters in various sizes Oaxaca (bulk)

Listeria monocytogenes contamination.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0920-2024
Lot/product code:
All dates through 05/02/2024 Oaxaca (bulk) PLU Batch ID 331 1AY-23307 331 1BY-23307 331 2AX-23307 331 2BX-23307 331 3AW-23307 331 3BW-23307 331 4AZ-23307 331 4BZ-23307 12331 3FZ-23310 331 3FZ-23310 331 1AY-23311 331 1BY-23311 331 2AX-23311 331 2BX-23311 331 3AW-23311 331 3BW-23311 331 4AZ-23311 331 4BZ-23311 56331 3EX-23311 56375 3DX-23311 331 3FW-23313 331 4FZ-23313 331 1CW-23314 331 2BZ-23314 331 3BY-23314 331 4BX-23314 331 4CX-23314 56331 2AW-23315 56331 4AY-23315 12331 2CY-23317 331 2CY-23317 331 3CX-23317 331 4BW-23317 331 1CW-23321 331 2BZ-23321 331 3BY-23321 331 4BX-23321 331 4CX-23321 12331 4BZ-23322 331 1AY-23322 331 1BY-23322 331 2AX-23322 331 2BX-23322 331 3AW-23322 331 3BW-23322 331 4AZ-23322 331 4BZ-23322 331 2EY-23324 337 4FW-23324 12331 4FY-23331 331 4FY-23331 331 1AY-23332 331 1BY-23332 331 2AX-23332 331 2BX-23332 331 3AW-23332 331 3BW-23332 331 4AZ-23332 331 4BZ-23332 331 3FW-23334 331 1AY-23335 331 1BY-23335 331 2AX-23335 331 2BX-23335 331 3AW-23335 331 3BW-23335 331 4AZ-23335 331 4BZ-23335 331 4FY-23338 337 3GZ-23338 331 1AX-23339 331 1BX-23339 331 2AW-23339 331 2BW-23339 331 3AZ-23339 331 4AY-23339 331 4BY-23339 331 1AY-23342 331 2AX-23342 331 3AW-23342 331 3BW-23342 331 4AZ-23342 51375 3BW-23342 56331 1BZ-23342 12331 3AW-23346 331 1AY-23346 331 1BY-23346 331 2AX-23346 331 2BX-23346 331 3AW-23346 331 3BW-23346 331 4AZ-23346 331 4BZ-23346 331 1AY-23349 331 1BX-23349 331 2AX-23349 331 2BW-23349 331 2CZ-23349 331 3AW-23349 331 3BZ-23349 331 3CY-23349 331 1AY-23350 331 1BX-23350 331 2AX-23350 331 2BW-23350 331 2CZ-23350 331 3AW-23350 331 3BZ-23350 331 3CY-23350 56331 1DX-23350 56375 3EY-23350 12331 4BZ-23353 331 1AY-23353 331 1BY-23353 331 2AX-23353 331 2BX-23353 331 3AW-23353 331 3BW-23353 331 4AZ-23353 331 4BZ-23353 331 1FY-23354 331 2EZ-23354 331 4FW-23354 331 1FZ-23355 331 2FY-23355 331 1AZ-23361 331 2AY-23361 331 2BY-23361 331 3AX-23361 331 3BX-23361 331 4BW-23361 331 4CW-23361 331 1AY-23364 331 2BZ-23364 331 3BY-23364 331 3CY-23364 331 4AZ-23364 337 2CZ-23364 12331 4BZ-24003 331 1AY-24003 331 1BY-24003 331 2AX-24003 331 2BX-24003 331 3AW-24003 331 3BW-24003 331 4AZ-24003 331 4BZ-24003 331 1AY-24006 331 2AX-24006 331 3AW-24006 331 4AZ-24006 331 1BZ-24008 331 2BY-24008 331 3BX-24008 331 4BW-24008 331 4CW-24008 331 1AY-24010 331 1BY-24010 331 2AX-24010 331 2BX-24010 331 3AW-24010 331 3BW-24010 331 4AZ-24010 331 4BZ-24010 331 2BY-24011 331 3BX-24011 51375 2CY-24011 56375 3CX-24011 331 1AZ-24016 331 2AY-24016 331 3AX-24016 331 4AW-24016 12331 4BZ-24020 331 1AY-24020 331 1BY-24020 331 2AX-24020 331 2BX-24020 331 3AW-24020 331 3BW-24020 331 4AZ-24020 331 4BZ-24020 12331 3CX-24023 331 1AZ-24023 331 1BZ-24023 331 2AY-24023 331 2BY-24023 331 3AX-24023 331 3BX-24023 331 3CX-24023 331 4AW-24023 331 4BW-24023 331 4CW-24023 331 1AZ-24025 331 1BZ-24025 331 2AY-24025 331 2BY-24025 331 3AX-24025 331 3BX-24025 331 3CX-24025 331 4AW-24025 331 4BW-24025 331 4CW-24025 331 1AW-24030 331 1BW-24030 331 2AZ-24030 331 3AY-24030 331 4AX-24030 12331 4BX-24033 331 1AW-24033 331 1BW-24033 331 2AZ-24033 331 2BZ-24033 331 3AY-24033 331 3BY-24033 331 4AX-24033 331 4BX-24033 56331 1EZ-23326
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)