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Recalls affecting Utah

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

16,456 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
FoodBacteria/virusRecalled February 17, 2022

Abbott EleCare Amino Acid-Based Powder Infant Formula with Iron 14.1oz. can, Abbott Elecare 400g. can, Abbott Elecare Unflavored 14.1oz. can. 6 cans per case. Item numbers: 55251 5525157 5525189 Retail UPCs: 070074535111 070074116297 070074119854

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0949-2022
Lot/product code:
Batches: 22331Z200 23377Z200 23438Z200 23439Z200 25562Z200 25562Z220 25563Z200 25729Z200 25730Z200 26731Z200 27922Z200 27931Z200 28124Z200 28125Z200 28126Z200 30291Z200 30292Z200 30517Z200 30518Z200 31392Z200 31402Z200 32421Z200 32684Z200 33694Z200 33695Z200 34012Z200 34769Z200 34770Z200 34771Z200 34771Z210 35023Z200 35032Z200 36149Z200 36150Z200 36151Z200 22331Z202 22331Z201
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Total Comfort 12.6oz. can. 6 cans per case. Item numbers: 6259962 Retail UPCs: 070074119953

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0921-2022
Lot/product code:
Batches: 35050K800
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Organic with A2 Milk Toddler Drink 23.2oz plastic jar. 4 jars per case. Abbott Similac Organic Toddler with A2 Milk Infant Formula with Iron 20.6oz. plastic jar. 4 jars per case. Item numbers: 67905 68104 Retail UPCs: 070074677576 070074681054

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0944-2022
Lot/product code:
Batches: 24399SH00 33780SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac 360 Total Care Infant Formula with Iron 20.6oz. and 30.3oz. palstic jar. 4 jars per case. 7oz. can. 6 cans per case. Item numbers: 68063 68065 68109 Retail UPCs: 070074680644 070074680668 070074681108

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0943-2022
Lot/product code:
Batches: 33737SH00 33738SH00 33739SH00 35974SH00 35975SH00 36097SH00 36229SH01 32372SH00 32435SH00 32436SH00 36085SH00 36230SH00 37314SH00 32592K800 32595K800 35011K800 36138K800 36139K800 36231K800 36232K800 37291K800 37313K800
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Pro-Total Comfort Infant Formula with Iron 20.1oz. and 22.5oz. plastic jar. 4 jars per case. 34oz. plastic jar. 6 jars per case. 7oz. can. 6 cans per case. Item numbers: 66798 66939 67925 68107 Retail UPCs: 070074667997 070074669403 070074679266 070074681085

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0934-2022
Lot/product code:
Batches: 26838SH00 26860SH00 26861SH00 30318SH00 31498SH00 31580SH00 33730SH00 24451SH00 24565SH00 26738SH00 26791SH00 23495K800 24481K800 25572K800 25588K800 26739K800 26837K800 28014K800 28141K800 28152K800 29243K800 29246K800 30319K800 31466K800 31579K800 31581K800 32613K800 32614K800 34860K800 36123K800 37236K800 27977SH00 27978SH00 27990SH00 28096SH00 28097SH00 30303SH00 30304SH00 31582SH00 31583SH00 33726SH00 33727SH00 33728SH00 33729SH00 37237SH00 37303SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Alimentum Infant Formula with Iron 12oz. can. 6 jars per case; 19.8oz. can. 4 cans per case; 7oz. can. 6 cans per case Item numbers: 64715 64717 64719 Retail UPCs: 070074647128 070074647166 070074647180

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0927-2022
Lot/product code:
Batches: 33691Z200 33692Z200 34758Z200 34759Z200 34759Z210 34776Z200 34777Z200 34778Z210 34930Z200 34931Z211 34932Z200 35015Z200 35016Z260 35033Z260 35034Z260 36035Z260 36036Z260 36067Z260 36068Z260 36155Z261 32420Z260 23380Z260 24464Z261 24528Z260 24529Z260 24533Z260 24534Z260 25661Z260 25661Z270 25662Z260 25663Z260 25664Z260 25725Z260 26726Z260 26727Z260 26728Z260 26732Z260 26733Z260 26805Z260 26806Z260 26807Z260 27925Z260 27941Z260 27942Z260 27943Z260 28042Z260 28042Z270 28043Z260 28044Z260 29260Z260 29261Z260 29262Z260 29268Z260 29269Z260 29270Z260 29271Z260 30286Z260 30287Z260 30375Z260 30376Z210 30377Z200 30378Z200 30379Z260 30380Z260 30381Z260 30382Z260 32404Z260 32405Z260 32417Z260 32418Z220 32419Z260 32424Z210 32424Z260 32425Z200 33426Z200 33427Z200 33428Z200 33696Z200 33697Z200 22332Z260 24496Z260 25559Z260 26813Z260 27929Z260 28045Z260 30288Z201 30383Z211 30383Z261 30386Z200 30387Z210 31403Z200 32418Z200 32418Z210 23381Z260 23381Z270 23382Z260 25551Z260 25552Z260 25553Z260 25554Z260 25555Z260 25556Z260 26814Z260 26815Z260 26816Z260 27868Z260 27869Z260 27870Z260 28117Z260 28118Z260 28119Z260 28120Z260 28121Z260 28122Z260 28136Z260 28137Z260 28138Z260 29187Z270 29188Z270 29189Z260 29190Z261 29259Z261 31413Z260 31414Z260 31415Z260 33698Z260 33699Z260 33700Z260 33700Z270 33701Z260 35017Z260 35018Z260 35019Z260 35020Z260 35021Z260 35022Z260
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Pro-Advance 20.6oz., 30.3oz., 34oz., and 658g plastic jar. 6 jars per case. 7oz. can. 6 cans per case. Item numbers: 6720113 6720813 6726613 6818013 6818213 6832313 Retail UPCs: 055325002499 055325002543 055325002604 055325002819 055325002833 055325003069

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0933-2022
Lot/product code:
Batches: 32624SH00 34958SH00 25673SH00 31463SH00 31549SH00 32625SH00 32626SH00 25604K800 31454K800 35008K800 37251K800 35055SH00 35056SH00 32624SH01 32625SH01 32626SH01
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 4, 2022

SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx Only, Manufactured for Fagron, Inc., St. Paul, MN 55120.

Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.

ALL 50 STATES
Full report

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

Recall #:
D-0856-2022
Lot/product code:
Lot #: a) A67185, Exp. Date 08/31/2024; b) Lot #: A67186, Exp. Date 08/31/2024
Recalling firm:
Fagron, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled March 30, 2022

Suave 24-Hour Protection Aerosol Antiperspirant Powder scent, Aluminum Chlorohydrate (19.1%), packaged in a) 4 oz. cans (UPC 0 79400 75150 8), and b) 6 oz. cans (UPC 0 79400 78490 2), Dist. By Unilever, Trumbull, CT 06611

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-0210-2024
Lot/product code:
all lots, expiry 9/30/2023
Recalling firm:
Unilever United States Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled May 24, 2022

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.

Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with not listed on the label diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.

ALL 50 STATES
Full report

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

Recall #:
D-1157-2022
Lot/product code:
Lot: LTARTKNGOMG30720, Exp Diciembre 2026
Recalling firm:
Walmart Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled October 20, 2022

Umami Everyday Sauce, 5 fl. oz. (148 mL) glass bottle, UPC 8-67732-00032-2, Made for Seed Ranch Flavor Co., LLC, Boulder, CO 80302 Ambient storage - minimum 35 degrees, maximum 85 degrees.

Three sauces contain not listed on the label soy.

ALL 50 STATES
Full report

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

Recall #:
F-0174-2023
Lot/product code:
Lot Codes: 010821 020921 030821 051721 081821 120321 012022 031422 042522 081822 092022
Recalling firm:
Seed Ranch Flavor Co
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled October 20, 2022

Umami Everyday Savory Spice, 5 fl. oz. (148 mL) glass bottle, UPC 8-50000-72724-3, Co-Packed with Seed Ranch Flavor Co., Denver, CO 80216 Ambient storage - minimum 35 degrees, maximum 85 degrees.

Three sauces contain not listed on the label soy.

ALL 50 STATES
Full report

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

Recall #:
F-0175-2023
Lot/product code:
Lot Codes: 120122 062521
Recalling firm:
Seed Ranch Flavor Co
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled October 20, 2022

Everything But The Sushi & Dumplings, 5 fl. oz. (148 mL) glass bottle, UPC 8-60008-58851-7, Made for Seed Ranch Flavor Co., LLC Boulder, CO 80302. Ambient storage - minimum 35 degrees, maximum 85 degrees.

Three sauces contain not listed on the label soy.

ALL 50 STATES
Full report

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

Recall #:
F-0176-2023
Lot/product code:
Lot Codes: 071122 081822 6188 BB061025
Recalling firm:
Seed Ranch Flavor Co
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled November 5, 2022

Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b) 8 fl. oz (237 mL) spray bottle, NDC 74943-125-08; c) 1 PINT / 16 fl. oz (475 ml.) spray bottle, NDC 74943-125-16; and d) 1 GALLON / 128 fl. oz. (3,785 ml.) jug, NDC 74943-125-28, Manufactured by B&B Blending, LLC, Northglenn, CO.

Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL BASED HAND SANITIZER isopropyl alcohol 75% v/v to contain methanol.

ALL 50 STATES
Full report

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

Recall #:
D-0066-2023
Lot/product code:
Lot: 133475
Recalling firm:
Adam's Polishes LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 30, 2023

Delsam Pharma's ARTIFICIAL TEARS (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1%, 1/2 fl oz (15 ml) bottle, Distributed By: Delsam Pharma Llc, Bronx, New York 10467, NDC 72570 121 15.

Non-Sterility: FDA analysis found unopened products to have bacterial contamination.

ALL 50 STATES
Full report

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

Recall #:
D-0921-2023
Lot/product code:
Lot #: PCMH001, PCMH002, PCMH005, PCMH007, Exp. date NOV-2023
Recalling firm:
Global Pharma Healthcare Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 30, 2023

Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/2 fl oz (15 ml) bottle, Distributed by. EzriCare, LLC, Lakewood, NJ, NDC 79503-0101-15.

Non-Sterility: FDA analysis found unopened products to have bacterial contamination.

ALL 50 STATES
Full report

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

Recall #:
D-0919-2023
Lot/product code:
Lot #: PCMI005, Exp. date AUG-2024; PCMJ001, PCMJ002, PCMJ004, PCMJ005, PCMJ006, PCMJ008, PCMJ009, PCMJ010, PCMJ011, PCMJ012, PCMJ013, PCMJ014, PCMJ015, Exp. date MAR-2025
Recalling firm:
Global Pharma Healthcare Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled February 14, 2023

Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution, 4fl. oz. [118mL], Distributed by Reliable Products, LLC, Cheyenne, WY 82003, NDC 75288-100-04.

Chemical Contamination: FDA analysis found the product to contain methanol, acetaldehyde, and acetal above the limits.

ALL 50 STATES
Full report

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

Recall #:
D-0455-2023
Lot/product code:
All Lots
Recalling firm:
Nanomaterials Discovery Corporation
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 14, 2023

Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034 91379 9; Manufactured by: Pharmedica USA, Phoenix, AZ.

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-0456-2023
Lot/product code:
Lot #s: a) 1808051, Exp.: 01/01/2027; b) 2203PS01, Exp.: 01/01/2027
Recalling firm:
Pharmedica USA, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 24, 2023

Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15%, White Petrolatum 83%), 3.5 grams (1/8 oz.) tube, Distributed By: Delsam Pharma Lic, Bronx, Newyork 10469, NDC 72570 122 35, UPC 3 72570 12235 3.

Non-Sterility: FDA analysis found unopened tubes to be contaminated with bacteria.

ALL 50 STATES
Full report

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

Recall #:
D-0488-2023
Lot/product code:
Batch # H29, Exp. Date 11/30/2023
Recalling firm:
Global Pharma Healthcare Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 13, 2023

Atovaquone Oral Suspension USP, 750 mg/5 mL, Packaged in 210 mL bottle, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured by: Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India, NDC# 31722-629-21.

Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.

ALL 50 STATES
Full report

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

Recall #:
D-0567-2023
Lot/product code:
Lot# E220182, Exp. 12/31/2023
Recalling firm:
Camber Pharmaceuticals Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 26, 2023

NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with not listed on the label sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this 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-0572-2023
Lot/product code:
Lot#: RO 927996, Exp: 12/25/2024
Recalling firm:
Gadget Island, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 26, 2023

DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with not listed on the label sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this 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-0573-2023
Lot/product code:
Lot/Item#: OMS760-B, Exp: 12/2025
Recalling firm:
Gadget Island, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 26, 2023

Pro Power Knight Plus capsule, 2550mg, 1-count blister card, Distributed by Beyond Health and youth Inc, Seattle, WA 98110, UPC 4 94922 90522 0.

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with not listed on the label sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this 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-0571-2023
Lot/product code:
No lot number, Exp: 06/2026
Recalling firm:
Gadget Island, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 3, 2023

Vegetal Vigra, 200mg capsules, 8-count bottle, Manufacturer: Hand-shaking (Int'l) Corp. USA ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA. UPC 8 931028 556885

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil an ingredient found in a FDA approved product for the treatment of male sexual enhancement, making this 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-1150-2023
Lot/product code:
All lots, Expires: 01/31/2025
Recalling firm:
APG SEVEN, INC
View official FDA record (opens in a new tab)
Class IHigh 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.

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-0037-2024
Lot/product code:
Lot: 6786, Exp: 03/31/25
Recalling firm:
Dr. Berne's Whole Health Products
View official FDA record (opens in a new tab)