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Recalls affecting Oregon

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

16,446 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
FoodBacteria/virusRecalled February 17, 2022

Abbott EleCare, EleCare LCP Hypoallergenic, Similac EleCare 400g. can. 6 cans per case. Item numbers: 5351034 5351066 5351039 5351077 Retail UPCs: 17703186031461 9340104000706 17501033957748 070074119281

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-0948-2022
Lot/product code:
Batches: 24549Z200 32429Z201 35025Z201 27871Z202 32429Z202 35025Z202 27871Z200 27871Z203 29258Z200 32429Z200 35025Z200 24549Z201 27871Z201 29258Z201 32429Z203
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac For Spit Up Infant Formula with Iron 22.5oz plastic jar. 6 jars per case. Item numbers: 5372976 Retail UPCs: 070074537306

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-0923-2022
Lot/product code:
Batches: 25667SH00 25668SH00 26872SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Human Milk Fortifier 0.9g Pouch / Sachet, 50 Pouch / Sachet per retail unit. 3 retail units per case Item numbers: 54598 5459813 5459814 5459820 5459886 6771009 Retail UPCs: 70074545998 070074545998 055325545996 070074109404 070074103297 070074671833

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-0919-2022
Lot/product code:
Batches: 22349Z200 25609Z200 26914Z200 26915Z200 26916Z200 26917Z200 26918Z200 26919Z200 26920Z200 26921Z200 27073Z200 28077Z200 28158Z200 28162Z200 28166Z200 29385Z200 30512Z200 30513Z200 30521Z200 31525Z200 31533Z200 31534Z200 31543Z200 32649Z200 32655Z200 32656Z200 32660Z200 32660Z210 32671Z200 33751Z200 33752Z200 34045Z200 34046Z210 34892Z200 34901Z200 35112Z200 35113Z200 35163Z200 36170Z200 30522Z200 32657Z200 22353Z200 22354Z200 26782Z200 26785Z200 27982Z200 27983Z200 31541Z200 33753Z200 34890Z200 34891Z200 35164Z200 36171Z200 24472Z200 25610Z200 27984Z200 32672Z200 32673Z200 32674Z200 22296Z200 22297Z200 25712Z200 26781Z200 26786Z200 26787Z200 30514Z200 30523Z200 31524Z200 31532Z200 31542Z200 32658Z200 33659Z200 33756Z200 33757Z200 34889Z200 36169Z200 22350Z200 22351Z200 22352Z200 22355Z200 22356Z200 22357Z200 23358Z200 23359Z200 24465Z200 24466Z200 24467Z200 24468Z200 24469Z200 24470Z200 24471Z200 25605Z200 25606Z200 25607Z200 25608Z200 25611Z200 25612Z200 25613Z200 25614Z200 25705Z200 25706Z200 25707Z200 25708Z200 25709Z200 25710Z200 25711Z200 25713Z200 25714Z200 26772Z200 26777Z200 26778Z200 26779Z200 26783Z200 26784Z200 26852Z200 26853Z200 27074Z200 27854Z200 27855Z200 27856Z200 27857Z200 27985Z200 27986Z200 28075Z200 28078Z200 28079Z200 28080Z200 28159Z200 28160Z200 28161Z200 28163Z200 28164Z200 28165Z200 30515Z200 30516Z200 30519Z200 30520Z200 31526Z200 31527Z200 31528Z200 31529Z200 31530Z200 31531Z200 31535Z200 31536Z200 31537Z200 31538Z200 31539Z200 31540Z200 32650Z200 32651Z200 32652Z200 32653Z200 32654Z200 32675Z200 33661Z200 33743Z200 33744Z200 33745Z200 33746Z200 33747Z200 33748Z200 33749Z200 33750Z200 33754Z200 33755Z200 33885Z200 33886Z200 34043Z200 34044Z200 34887Z200 34888Z200 34893Z200 34894Z200 34895Z200 34896Z200 34897Z200 34898Z200 34899Z200 34900Z200 34902Z200 34903Z200 34904Z200 34905Z200 35110Z200 35111Z200 28076Z200
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 Infant Formula with Iron 12.6oz. can. 6 cans per case. Item numbers: 62599 Retail UPCs: 070074626000

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-0939-2022
Lot/product code:
Batches: 24449K800 24449K801 24450K800 24482K800 24515K800 24516K800 24566K800 24566K801 25571K800 25571K801 25650K800 25651K800 25687K800 25688K800 26747K800 26748K800 26817K800 26818K800 26819K800 26830K800 26832K800 26834K800 26835K800 27888K800 27889K800 27890K800 27891K800 27951K800 28017K800 28086K800 28088K800 28098K800 28178K800 28179K800 28179K801 28180K800 29219K800 29220K801 29237K800 29238K800 30314K800 30316K800 30317K800 31467K800 31468K800 31469K800 31470K800 31584K800 31586K800 32609K800 32611K800 32612K800 33706K800 33706K801 33707K800 33708K800 34073K800 34800K800 34801K800 34844K800 34844K801 34845K800 34846K800 34847K800 34865K800 34866K800 34867K800 34868K800 34869K800 34870K800 34943K800 34944K800 35981K800 35982K800 35983K800 36086K800 36121K800 36122K800 36212K800 36213K800 37238K800 37239K800 37240K800 37241K800 37298K800 37299K800 37300K800 37301K800 37302K800 37430K800 37431K800
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 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

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

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

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
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
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
FoodRecalled April 13, 2023

Highkey soft baked MINI TREATS BANANA NUT MUFFIN NET WT 2 OZ (57g) CONTAINS: ALMONDS, MILK, AND PECANS. DISTRIBUTED BY SUMMIT NATURALS INC ORLANDO, FL 32826 UPC 8 50020 43373 5

The firm was notified that a consumer had an allergic reaction to their product. The product did not list egg on the label.

CACOFLKYNJORWA
▸Full report

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

Recall #:
F-0884-2023
Lot/product code:
2216101 JUN102023
Recalling firm:
SUMMIT NATURALS INC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 13, 2023

Highkey Soft Baked MINI TREATS BIRTHDAY CAKE NET WT 2 OZ (57g) CONTAINS: ALMONDS, MILD, AND COCONUT. DISTRIBUTED BY SUMMIT NATURALS INC ORLANDO, FL 32826 UPC 8 50020 43374 2

The firm was notified that a consumer had an allergic reaction to their product. The product did not list egg on the label.

CACOFLKYNJORWA
▸Full report

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

Recall #:
F-0885-2023
Lot/product code:
2216101 JUN102023
Recalling firm:
SUMMIT NATURALS 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
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
FoodBacteria/virusRecalled June 23, 2023

FABRIQUE' EN CORSE TOMME CORSE AU LAIT DE BREBIS***ANTOINE OTTAVI FROMAGER***aFFINAGE 3 A' 5 MOIS SARL Fromagerie Ottavi 20240 Ghisonaccia Corsica

Possible microbiological contamination, specifically Listeria monocytogenes.

OR
▸Full report

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

Recall #:
F-1383-2023
Lot/product code:
LOT#: VC349 BBD: 08/05/2023
Recalling firm:
Estancia Holdings
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
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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)