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Recalls affecting Puerto Rico

Data last updated: September 9, 2026 at 1:18 PM UTC

16,258 recalls found
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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/virusSalmonellaAnnounced 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/virusE. coliAnnounced 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)
UnclassifiedAllergenMilkUndeclaredAnnounced 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/virusSalmonellaE. coliAnnounced 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/virusSalmonellaAnnounced 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)
Wording
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 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, 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

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
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
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
DrugRecalled August 9, 2023

Blis-To-Sol Liquid (Tolnaftate), 1%, packaged in a) 1 FLUID OZ. (29.5 mL) bottles, UPC 0 11169 20011 8 and b) 1.85 FLUID OZ. (54.5 mL) bottles, UPC 0 11169 20012 5, Distributed by Oakhurst Company, Levittown, NY 11756.

CGMP Deviations: Products not manufactured under current good manufacturing practices.

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-1096-2023
Lot/product code:
Lot: 9E098A
Recalling firm:
Ecometics, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 9, 2023

Lugol's (Strong Iodine Solution USP), Each mL contains Iodine 0.05gm and potassium iodide 0.100gm, 8mL Single Use Vials, Rx Only, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6064-0, Ref 6064.

CGMP Deviations: Products not manufactured under current good manufacturing practices.

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-1102-2023
Lot/product code:
Lot #: 2E235A, exp: 2/2024; 2E293A, exp: 3/2024
Recalling firm:
Ecometics, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 9, 2023

Unguentine Ointment, (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Zinc Oxide 6.6%), labeled as a) NET WT 1 OZ (28 g) tubes, Improved Formula, UPC 0 11169 10216 0, and b) NET WT 1 OZ (28.3g) tubes, Maximum Strength, UPC 0 11169 11250 3, Distributed by: Oakhurst Company, Levittown, NY 11756.

CGMP Deviations: Products not manufactured under current good manufacturing practices.

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-1099-2023
Lot/product code:
a) and b) 1E113A, exp 4/24
Recalling firm:
Ecometics, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 9, 2023

activator concentrate, Sodium Fluoride 0.96% in Activator Concentrate; 0.08% in diluted Activator Solution, Net 1 FL. OZ., Manufactured for: All USA Direct, LLC, Broadview, IL 60155.

CGMP Deviations: Products not manufactured under current good manufacturing practices.

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-1100-2023
Lot/product code:
Lot: 1E175B, exp 6/24
Recalling firm:
Ecometics, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 9, 2023

YAGER'S LINIMENT (Camphor and Turpentine Oil) 3.1% and 8.12% respectively, packaged in a) 4 FL OZ (118 mL) bottles, UPC 0 11169 00004 6, and 8 FL OZ (236 mL) bottles, UPC 0 11169 00008 4, The Oakhurst Co., Dist., Levittown, NY 11756.

CGMP Deviations: Products not manufactured under current good manufacturing practices.

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-1097-2023
Lot/product code:
Lot: 0E267A
Recalling firm:
Ecometics, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 9, 2023

AstrinGyn (Ferric Subsulfate) Aqueous, 259 mg/g, 8 gm Single Use Vials, Manufactured for CooperSurgical, Trumbull, CT 06611, NDC 59365-6065-0, Ref 6065.

CGMP Deviations: Products not manufactured under current good manufacturing practices.

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-1101-2023
Lot/product code:
Lot #: 2E144A, 2E157A, exp: 11/2023; 2E270A, exp: 3/2024; 2E300A, exp: 4/2024
Recalling firm:
Ecometics, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 9, 2023

ALCOLADO RELAMPAGO (Menthol and Camphor), 1% and 1.5% respectively, packaged in a 7 FLUID OZ (207 ml) bottles, UPC 7 18864 20102 9 and b) 16 FLUID OZ (472 ml) bottles, UPC 7 18864, 20110 4, Distributed by: The Larkspur Group, Inc., Norwalk, CT 06854.

CGMP Deviations: Products not manufactured under current good manufacturing practices.

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-1098-2023
Lot/product code:
a) 0E280A, exp 10/23; 0E318A, exp 11/23; 1E109A, exp 3/24; 1E141A, exp 5/24; b) 0E280A, exp 11/23; 1E109A, 1E141A, exp 3/24
Recalling firm:
Ecometics, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 14, 2023

All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.

CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center. Also, due to unusually hot weather, FDA Recalled Products may have been subjected to temperatures in excess of storage condition instructions on product labeling.

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-1104-2023
Lot/product code:
Miscellaneous
Recalling firm:
Inmar Supply Chain Solutions, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 18, 2023

Humanrace Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, packaged as a 148mL (5 fl oz.) bottle, PA ++++, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Squalene, Aloe, Dist. By: @Humanrace 2022 Beverly Hills, CA 90210, USA, NDC 82779-002

Weaker than it should be Drug: Product does not contain SPF that is declared on the label.

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-1176-2023
Lot/product code:
Lot #: 1752A, 1752B, 1782E, 1782G, 1782C, 1752C, 1782B; Exp. 06/2024.
Recalling firm:
HUMANRACE
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusListeriaRecalled August 18, 2023

Individually Quick Frozen (IQF) Corn distributed in BULK TOTES (1650lbs and 1750lbs) to consignees for further processing. Bulk tote labels have cooking instructions. Individually Quick Frozen (IQF) Super Sweet Corn, foodservice item, packaged in 32oz. plastic bag, 12 bags per case. The poly bag is stamped with lot code and Product of USA. No UPC. Individually Quick Frozen (IQF) Super Sweet Cut Corn, food service item, packaged in 40oz. poly bags, 12 bags per case. The poly bag is clear (no printing except the coding). Master case label declares KFC Super Sweet Cut Corn, 12-40oz bags, 30lbs. UPC 885251248124.

Listeria monocytogenes

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 #:
F-1503-2023
Lot/product code:
Bulk Totes: Shop Orders 21369 and 21373. Manufactured on 8/21/2022. Corn 32oz: 83012. KFC Corn 40oz: Use by Oct 24 2024 82972 554922 822315.
Recalling firm:
Twin City Foods, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 18, 2023

Humanrace Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30, packaged as a 53mL (1.8 fl oz.) bottle, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Dist. By: @Humanrace 2022 Beverly Hills, CA 90210, USA, NDC 82779-01

Weaker than it should be Drug: Product does not contain SPF that is declared on the label.

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-1175-2023
Lot/product code:
Lot #: 1732A, 1732B, 1742A, 1742B, 1742C, 1742D; Exp. 06/2024.
Recalling firm:
HUMANRACE
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusListeriaRecalled August 18, 2023

Mixed Vegetables BEST PRICE TOPVALU, net per bag 500g. Label is in foreign language. 4549414484120 Food Lion Mixed Vegetables Carrots, Corn, Green Beans & Peas. Product of USA, net wt. per bag 16oz, 12 bags per case. Distributed by Food Lion, LLC Salisbury, NC. UPC 35826005090 Kroger Mixed Vegetables Carrots, Super Sweet Corn, Green Beans & Green Peas. Product of USA, net wt. per bag 12oz, 14 bags per case. Distributed by The Kroger C. Cincinnati, OH. UPC 11110849625 Kroger Mixed Vegetables Carrots, Super Sweet Corn, Green Beans & Green Peas. Product of USA, net wt. per bag 32oz, 6 bags per case. Distributed by The Kroger C. Cincinnati, OH. UPC 11110865854

Listeria monocytogenes

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 #:
F-1506-2023
Lot/product code:
BEST PRICE TOPVALU: 2025.01.06 Food Lion: 50183 BEST BY 18 JAN 2025 Kroger 12oz: 53122 BEST IF USED BY MAY 2024 53412 BEST IF USED BY JUN 2024 BEST IF USED BY APR.2024 82942 BEST IF USED BY APR.2024 83012 BEST IF USED BY AUG.2024 80463 Kroger 32oz. BEST IF USED BY FEB.2024 82352
Recalling firm:
Twin City Foods, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusListeriaRecalled August 18, 2023

Individually Quick Frozen (IQF) Corn, distributed in bulk cases (1kg, 10kg, 12kg, 15kg, 25kg) to consignees for further processing. Cases are read in parts: Product of U.S.A. Packed By Twin City Foods, Inc. Stanwood, Washington. Super Sweet Grade A Cut Corn Blanched Vegetables, net wt. 12kg (12/1kg bags per case). Super Sweet Grade A Cut Corn Blanched Vegetable, net wt. 10kg Super Sweet Cut Corn Blanched Vegetables, net wt. 12kg Super Sweet Cut Corn Blanched Vegetables, LARGE, net wt. 12kg Super Sweet Grade A Cut Corn Blanched Vegetables, net wt. 15kg Super Sweet Grade A Triple Clean Cut Corn Blanched Vegetables, net wt. 15kg Super Sweet Grade A Cut Corn Blanched Vegetables, net wt. 25kg Super Sweet Grade A Triple Clean Cut Corn, net wt. 25kg

Listeria monocytogenes

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 #:
F-1504-2023
Lot/product code:
BULK CASES have the following codes and USE BY DATES: Super Sweet Grade A Cut Corn Blanched Vegetables, net wt. 12kg (12/1kg bags per case) has the USE BY dates: 2024.12.21 81723 2024.12.23 81743 2025.01.03 81843 Super Sweet Corn, net wt. 10kg, has the USE BY dates: 2025.06.22 31733 553293 330695 2025.06.23 31743 553293 330697 Super Sweet Cut Corn Blanched Vegetables, net wt. 12kg, has the USE BY dates: 2024.12.28 33622 553062 330246 2025.05.26 31463 553062 330621 2025.05.31 31513 553062 330633 Super Sweet Cut Corn Blanched Vegetables, LARGE, net wt. 12kg, has the USE BY dates: 2024.12.06 33402 553172 330193 2024.12.07 33412 553172 330197 2024.12.15 33492 553172 330227 2025.01.06 30063 553172 330266 2025.01.10 30103 553172 330275 2025.01.09 30093 553172 330270 2025.01.11 30113 553172 330279 2025.01.19 30193 553172 330311 2025.01.20 30203 553172 330313 2025.01.24 30243 553172 330329 2025.01.27 30273 553172 330342 2025.01.30 30303 553172 330347 2025.02.01 30323 553172 330355 2025.06.27 31783 553173 330703 Super Sweet Corn, net wt. 15kg, has the USE BY dates: 2025.05.15 31353 553032 330599 Super Sweet Corn Triple Clean, net wt. 15kg, has the USE BY dates: USE BY 2025.03.01 30603 555472 330407 USE BY 2025.06.19 31703 555473 330681 Super Sweet Cut Corn, net wt. 25kg, has the USE BY dates: USE BY 2025.05.10 31303 551932 330588 USE BY 2025.05.12 31323 551932 330595 Super Sweet Grade A Triple Clean Cut Corn, net wt. 25kg, has the USE BY dates: 2025.02.09 30403 553012 330377 2025.03.01 30603 553012 330409 2025.03.03 30623 553012 330415 2025.04.19 31093 553012 330534 2025.05.11 31313 553012 330592 2025.05.12 31323 553012 330596 2025.05.17 31373 553012 330605 2025.05.30 31503 553012 330630
Recalling firm:
Twin City Foods, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusListeriaRecalled August 18, 2023

Kernel Corn, BEST PRICE TOPVALU, net wt. per bag 300g. Label is in foreign language. UPC 4549414086232 Signature Select Golden Corn Super Sweet, Product of USA, net wt. per bag 12oz, 12 bags per case. UPC 21130090655 Food Lion Super Sweet Cut Yellow Corn, Product of USA, net wt. per bag 16oz, 12 bags per case. Distributed by Food Lion, LLC Salisbury, NC. UPC 35826079855 Kroger Super Sweet Corn, Product of USA, net wt. per bag 12oz, 14 bags per case. Distributed by The Kroger C. Cincinnati, OH. UPC 11110849618 Kroger Super Sweet Corn, Product of USA, net wt. per bag 32oz, 6 bags per case. Distributed by The Kroger C. Cincinnati, OH. UPC 11110865786

Listeria monocytogenes

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 #:
F-1505-2023
Lot/product code:
BEST PRICE TOPVALU: 2024.02.23 Signature Select: BEST IF USED BY FEB.22.24 S5716 Food Lion: 53072 BEST BY 03 NOV 2024 Food Lion: 53622 BEST BY 28 DEC 2024 Kroger 12oz: 52842 BEST IF USED BY APR 2024 53042 BEST IF USED BY APR 2024 53272 BEST IF USED BY MAY 2024 53542 BEST IF USED BY JUN 2024 50043 BEST IF USED BY JUL 2024 50033 BEST IF USED BY JUL 2024 BEST IF USED BY APR.2024 82842 BEST IF USED BY FEB.2024 82352 Kroger 32oz. 53052 BEST IF USED BY MAY 2024 53112 BEST BY MAY 2024 BEST IF USED BY APR.2024 82932 BEST IF USED BY APR.2024 83012
Recalling firm:
Twin City Foods, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 25, 2023

BD ChloraPrep Clear, 2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) Sterile Solution, 0.03mL (1 ml) each, 60 applicators in carton, applicator is sterile if package is intact. CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co., NDC 54365-400-31 REF 930480 Product is packaged in the following manner: There is one (1) sterile applicator (sponge) per pouch. Each inner carton contains sixty (60) pouches. There are four (4) inner cartons per shipping case (total of 240 pouches per case).

Stability data does not support expiry: Shelf-life of the impacted lots of BD ChloraPrep" Clear 1 mL Applicator cannot be substantiated beyond 12-months although labeled with 36-month expiry. Stability studies indicate that the impacted lots, if stored at 30¿C/75% relative humidity continuously beyond 12 months, may exhibit growth of Aspergillus penicillioides.

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

Recall #:
D-1168-2023
Lot/product code:
Lot # 2272350, Exp. Date 09/30/2025 and Lot # 2301939, Exp. Date 09/30/2025
Recalling firm:
CareFusion 213, LLC
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Class IIModerate risk
DrugRecalled August 26, 2023

Dr. Berne's Organic Castor Oil Eye Drops, Net WT 30 mL/1 fl oz bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, hello@drsamberne.com, Certified Organic by Organic Certifiers.

CGMP Deviations

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

Recall #:
D-0035-2024
Lot/product code:
Lot: 6666, Exp. 11/30/25
Recalling firm:
Dr. Berne's Whole Health Products
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Class IIModerate risk
DrugRecalled August 26, 2023

Dr. Berne's MSM MIST 15% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, hello@drsamberne.com.

CGMP Deviations

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

Recall #:
D-0034-2024
Lot/product code:
Lot: 6617, Exp. 05/24; 6623, Exp 06/24; 6646, Exp 07/24; 6675, Exp 09/24; 6716, Exp 11/24.
Recalling firm:
Dr. Berne's Whole Health Products
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled August 26, 2023

Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, hello@drsamberne.com, UPC 00854582001111.

CGMP Deviations

ALL 50 STATES
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A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0036-2024
Lot/product code:
Lot: 6485, Exp: 11/23: 6562, Exp: 03/24; 6624, Exp: 06/24; 6669, Exp: 08/24; 6688, Exp: 09/24; 6727, EXP: 11/24; 6771, Exp: 02/25; 6830, Exp: 03/25; 6887, Exp: 07/25.
Recalling firm:
Dr. Berne's Whole Health Products
View official FDA record (opens in a new tab)