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Recalls affecting Rhode Island

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

16,151 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
DrugUndeclaredRecalled April 14, 2025

ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.

Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with not listed on the label propoxyphenylsildenafil and sildenafil.

ALL 50 STATES
Full report

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

Recall #:
D-0466-2025
Lot/product code:
All lots Lot #: KT-1ST-43-01-10/2025, Exp. 01/10/2027
Recalling firm:
SAINI TRADE INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 14, 2025

Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.

Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with not listed on the label propoxyphenylsildenafil and sildenafil.

ALL 50 STATES
Full report

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

Recall #:
D-0467-2025
Lot/product code:
All lots Lot #: KT-1ST-43-0110/2025, Exp. 03/15/2026
Recalling firm:
SAINI TRADE INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 14, 2025

MALEXTRA, Recharge with Extra, Dietary Supplement, 10 capsules per box, Distributed by: Health Fixer, Tempe, AZ 85288, UPC B0CWKZ6ZP3.

Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with not listed on the label propoxyphenylsildenafil and sildenafil.

ALL 50 STATES
Full report

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

Recall #:
D-0464-2025
Lot/product code:
All lots Lot #: KT-1ST-43-01-04/2026, Exp. 04/25/2026
Recalling firm:
SAINI TRADE INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 14, 2025

Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.

Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with not listed on the label propoxyphenylsildenafil and sildenafil.

ALL 50 STATES
Full report

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

Recall #:
D-0463-2025
Lot/product code:
All Lots Lot #: KT-1ST-43-01-10-2025, Exp. 01/10/2027
Recalling firm:
SAINI TRADE INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 14, 2025

ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.

Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with not listed on the label chloropretadalafil, propoxyphenylsildenafil, and sildenafil.

ALL 50 STATES
Full report

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

Recall #:
D-0465-2025
Lot/product code:
All lots Lot #: KT-1ST-43-01-07/2024, Exp. 10/15/2026
Recalling firm:
SAINI TRADE INC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 13, 2025

Levetiracetam 0.75% in Sodium Chloride Injection 1,000 mg/100 mL (10 mg/mL), 1 x 100mL, Rx Only, Manufactured by: Gland Pharma Limited, Hyderabad, - 500 043 INDIA, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, NDC 43598-636-52

LABELING: LABEL MIX-UP: The infusion bag is incorrectly labeled as Levetiracetam in 0.82% Sodium Chloride Injection 500 mg/100 mL, while the aluminum overwrap packaging correctly identifies the product as Levetiracetam in 0.75% Sodium Chloride Injection 1,000 mg/100 mL.

ALL 50 STATES
Full report

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

Recall #:
D-0365-2025
Lot/product code:
Lot: A1540076, Exp 08/31/2026
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Strawberry Shake (4 oz), UPC 10045796017358; Imperial Strawberry Shake (4 oz), UPC 00074865927017

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0654-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Strawberry Shake Plus (4 oz), UPC 10045796017495

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0661-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Vanilla Shake Plus (4 oz), UPC 10045796017549

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0662-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Strawberry Shake No Sugar Added (4 oz), UPC 10045796017372; Imperial Strawberry Shake No Sugar Added (4 oz), UPC 00074865926843

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0657-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Vanilla Shake No Sugar Added (4 oz), UPC 10045796017365; Imperial Vanilla Shake No Sugar Added (4 oz), UPC 00074865927031

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0659-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Strawberry Banana Shake No Sugar Added (4 oz), UPC 10045796018447; Imperial Strawberry Banana Shake No Sugar Added (4 oz), UPC 00074865987325

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0658-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Vanilla Shake (4 oz), UPC 10045796017334; Imperial Vanilla Shake (4 oz), UPC 00074865926836

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0655-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Chocolate Shake Plus (4 oz), UPC 10045796017471

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0660-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Chocolate Shake No Sugar Added (4 oz), UPC 10045796036335; Imperial Chocolate Shake No Sugar Added (4 oz), UPC 10734730244720

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0656-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 21, 2025

Ready Care Chocolate Shake (4 oz), UPC 10045796017341; Imperial Chocolate Shake (4 oz), UPC 00074865926997

Potential contamination with Listeria monocytogenes.

ALL 50 STATES
Full report

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

Recall #:
F-0653-2025
Lot/product code:
BB codes: 022125 to 022126
Recalling firm:
Lyons Magnus LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled February 20, 2025

Vitality, Fast Acting Male Enhancement Product, Dietary Supplement, a) One Capsule per Packet, b) 6 capsules per bottle, Xtreme Potency.

Marketed without an approved NDA/ANDA: Product found to be tainted with not listed on the label sildenafil and tadalafil.

ALL 50 STATES
Full report

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

Recall #:
D-0281-2025
Lot/product code:
All lots
Recalling firm:
One Source Nutrition, Inc,
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 20, 2025

PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, 855-275-2270, NDC 71285-6092-1.

Presence of Particulate Matter

ALL 50 STATES
Full report

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

Recall #:
D-0272-2025
Lot/product code:
Lot 37-928390, Exp Date, 03MAR2025; Lot 37-928796, Exp Date, 09MAR2025; Lot 37-928839, Exp Date, 10MAR2025
Recalling firm:
Central Admixture Pharmacy Services, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 14, 2025

BD ChloraPrep Clear 1mL Applicators, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, 0.03 fl. oz (1 mL) each, 60 Applicators per Carton, CareFusion 213, LLC, El Paso, TX 79912, Subsidiary of Becton, Dickinson and Co., REF 930480, NDC 54365-400-31.

Non-Sterility: contamination of Aspergillus penicillioides, due to breach in package lidding.

ALL 50 STATES
Full report

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

Recall #:
D-0259-2025
Lot/product code:
Lot #: 3200240, Exp 6/30/2026
Recalling firm:
CareFusion 213, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 13, 2025

POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL, 100 mEq/L flexible container, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26; Bar Code (01)00309907074269

Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium Chloride Inj 10 mEq may contain flexible containers of Potassium Chloride Inj 20 mEq

ALL 50 STATES
Full report

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

Recall #:
D-0268-2025
Lot/product code:
Lot 1023172, Exp Date: 31 January 2026
Recalling firm:
ICU Medical, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 13, 2025

POTASSIUM CHLORIDE Inj., 20 mEq total in 100 mL flexible container 24 x case, 200 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7075-26; Bar Code Flexible container (01) 00309907075266; Case (01)30309907075267

Labeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE 20 mEq, may contain flexible containers with overwrap mislabeled as 10 mEq. The correct dosage strength of 20 mEq is printed on the labeling affixed to the product flexible container.

ALL 50 STATES
Full report

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

Recall #:
D-0267-2025
Lot/product code:
Lot 1023172, Exp Date: 31 January 2026
Recalling firm:
ICU Medical, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 31, 2025

Fentanyl Transdermal System CII, 25mcg/h, packaged in a pouch, further packaged in 5-count carton, Rx only, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058, Manufactured by: Kindeva Drug Delivery L/P, Northridge, CA 91324, NDC 47781-424-47.

Defective delivery system - patches could be multi-stacked, adhered one on top of the other, in a single product pouch.

ALL 50 STATES
Full report

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

Recall #:
D-0245-2025
Lot/product code:
Lot #: 108319, Exp: 04/30/2027
Recalling firm:
Alvogen, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugBacteria/virusRecalled January 28, 2025

SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 Soft tip Squeeze Bottle, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00104 1

Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus

ALL 50 STATES
Full report

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

Recall #:
D-0299-2025
Lot/product code:
Lot# 024122661Al, Exp Date 12/2027
Recalling firm:
Ascent Consumer Products Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugBacteria/virusRecalled January 28, 2025

SinuCleanse Soft Tip NETI POT Nasal Wash System (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg), 30-count All Natural USP Grade Saline Packets and 1 kettle style Neti Pot, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00102 7

Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus

ALL 50 STATES
Full report

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

Recall #:
D-0301-2025
Lot/product code:
Lot# 024122661Al, Exp Date 12/2027
Recalling firm:
Ascent Consumer Products Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugBacteria/virusRecalled January 28, 2025

SinuCleanse Premixed SALINE PACKETS (sodium bicarbonate USP 700 mg and sodium chloride USP 2300 mg) for Nasal Wash System, 60-count All Natural USP Grade Saline Packets, Net WT 0.1OZ (3g) each, Distributed by Ascent Consumer Products Inc., Melville, NY 11747, UPC 6 46011 00103 4

Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus

ALL 50 STATES
Full report

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

Recall #:
D-0300-2025
Lot/product code:
Lot# 024122661Al, Exp Date 12/2027
Recalling firm:
Ascent Consumer Products Inc.
View official FDA record (opens in a new tab)