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Recalls affecting Florida

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

17,355 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 Men — dietary 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 Alive — Moringa 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. Braun — 0.9% 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 Value — Organic 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

Lipofit — Lipofit 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

Kofinas — Garlic 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 Temptations — Chocolatey 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 Sprouts — Robust 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

Martina — Mangoes

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)
NewestOldest
High riskLow riskAll
Wording
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, ORANGE BOX.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1168-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL TEJOCOTE ROOT 90 PIECES, 3 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1161-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL TEJOCOTE ROOT Dietary Supplement Net WT 0.36 oz (10g)

Product is being recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1158-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 & 03/24
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, ORANGE BOTTLE.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1172-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOX, 2 ORANGE BOXES.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1162-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOX, 2 YELLOW BOXES

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1165-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOX, 2 BLACK BOXES.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1170-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL TEJOCOTE ROOT TWO PACK 180 PIECES, 6 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1160-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, YELLOW BOX.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1169-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

Brazil Seed Net WT 0.18 oz (5g)

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1159-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, YELLOW BOTTLE.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1167-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOTTLE, 2 BLACK BOTTLES.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1163-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL 2 PACK! BRAZIL SEED 30 PIECES, FOR 30 DAYS, 5 GRAMS PER BOX

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1164-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, BLACK BOX.

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1171-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 9, 2024

H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, BLACK BOTTLE

Product recalled due to the presence of yellow oleander and its components in the product.

ALL 50 STATES
▸Full report

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

Recall #:
F-1166-2024
Lot/product code:
No Lot code on label. Expiration date listed as 05/24 and 03/24.
Recalling firm:
HandNatural
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled February 6, 2024

SCHWINNNG Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Today the World LLC, Vancouver, WA 98683

Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with not listed on the label nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this drug an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-0344-2024
Lot/product code:
Lot #: 2108, Exp. Date 10/31/2024.
Recalling firm:
Today The World
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled February 6, 2024

Sustain Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by VSD Productions, Inc. Las Vegas, Nevada

Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be tainted with not listed on the label tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this drug an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-0343-2024
Lot/product code:
Lot #: BTH:230551, Exp. Date 12.05.2026; BTH:230571, Exp. Date 14.05.2026
Recalling firm:
Today The World
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled February 6, 2024

Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001, www.getarize.com

Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with not listed on the label nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this drug an unapproved drug.

ALL 50 STATES
▸Full report

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

Recall #:
D-0345-2024
Lot/product code:
Lot #: 2107, Exp. Date 10/31/2024.
Recalling firm:
Today The World
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled February 1, 2024

RAM IT, Horny Goat Weed, dietary supplement capsules, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026

Marketed Without an Approved NDA/ANDA: Products contain not listed on the label sildenafil.

ALL 50 STATES
▸Full report

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

Recall #:
D-0585-2024
Lot/product code:
Lot HGW221116 (Batch 020123-1), Exp 5/31/2025
Recalling firm:
Integrity Products
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled February 1, 2024

TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591 UPC 3 63736 81961 3

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-0346-2024
Lot/product code:
Lot # 0H50545, Exp. date 07/31/24; 1G50645, Exp. date 06/30/25
Recalling firm:
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled February 1, 2024

To the Moon Capsules, Horny Goat Weed, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026

Marketed Without an Approved NDA/ANDA: Products contain not listed on the label sildenafil.

ALL 50 STATES
▸Full report

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

Recall #:
D-0586-2024
Lot/product code:
Lot HGW221116 (Batch 022123-1), Exp 5/31/2025
Recalling firm:
Integrity Products
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 12, 2024

Neptune's Fix, Tianeptine Tablets Extended Relief, Twenty Tablets per Box, Wide Awake, 3000 mg (150 mg Per Tablet), Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

ALL 50 STATES
▸Full report

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

Recall #:
D-0335-2024
Lot/product code:
All lots
Recalling firm:
Neptune Resources, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 12, 2024

Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

ALL 50 STATES
▸Full report

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

Recall #:
D-0333-2024
Lot/product code:
All lots
Recalling firm:
Neptune Resources, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 12, 2024

Neptune's Fix, Tianeptine Extra Strength Elixir, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

ALL 50 STATES
▸Full report

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

Recall #:
D-0334-2024
Lot/product code:
All lots
Recalling firm:
Neptune Resources, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 11, 2024

Tio Francisco Yogurt (Plain, Strawberry, Peach, Mango) Available to consumers at retail deli counters in various sizes

Listeria monocytogenes contamination.

ARAZCACOFLGAIAILKSMDNCNJNVNYORRITXUTVAWA
▸Full report

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

Recall #:
F-0926-2024
Lot/product code:
All dates through 04/17/2024 PLU Batch ID 773 B1-23319-Stirred Yogurt Mango 771 B1-23319-Stirred Yogurt Peach 770 B1-23319-Stirred Yogurt Strawberry 773 B1-23333-Stirred Yogurt Mango 771 B1-23333-Stirred Yogurt Peach 770 B1-23333-Stirred Yogurt Strawberry 773 B1-23354-Stirred Yogurt Mango 771 B1-23354-Stirred Yogurt Peach 770 B1-23354-Stirred Yogurt Strawberry 773 B1-23362-Stirred Yogurt Mango 771 B1-23362-Stirred Yogurt Peach 770 B1-23362-Stirred Yogurt Strawberry 773 B1-2411-Stirred Yogurt Mango 771 B1-2411-Stirred Yogurt Peach 446 B1-2411-Stirred Yogurt Plain 770 B1-2411-Stirred Yogurt Strawberry 773 B1-2419-Stirred Yogurt Mango 771 B1-2419-Stirred Yogurt Peach 770 B1-2419-Stirred Yogurt Strawberry 773 B1-2432-Stirred Yogurt Mango 771 B1-2432-Stirred Yogurt Peach 446 B1-2432-Stirred Yogurt Plain 770 B1-2432-Stirred Yogurt Strawberry
Recalling firm:
Rizo Lopez Foods, Inc. dba Don Francisco Cheese
View official FDA record (opens in a new tab)