BIGNOPE
Ko-fi

Recalls affecting Virginia

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

16,858 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 Infant Formula Powder 12.6oz. can. 6 cans per case. Item numbers: Clinical Retail UPCs: N/A - Clinical

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-0957-2022
Lot/product code:
Batches: 29169K800
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
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Sensitive 34oz. plastic jar. 6 jars per case. Abbott Similac Sensitive Infant Formula with Iron 12.5oz. can and 20.1oz. plastic jar. 6 units per case. Item numbers: 68082 5753978 6748901 674891L Retail UPCs: 070074680835 070074575414 070074122380

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-0938-2022
Lot/product code:
Batches: 28015SH00 28013SH00 28016SH00 28018SH00 28019SH00 30302SH00 30447SH00 30449SH00 32610SH00 36214SH00 36215SH00 23390K800 23392K800 23422K800 23423K800 23424K800 23425K800 23428K800 23429K800 24454K800 24455K800 24483K800 24484K800 24485K800 24486K800 24487K800 24488K800 24504K800 24505K800 24506K800 24517K800 25591K800 25592K800 25678K800 25678K801 25679K800 25734K800 25735K800 26741K800 26743K800 26745K800 26788K800 26789K800 27879K800 27892K800 27893K800 27947K800 27948K800 27949K800 27950K800 27952K800 28020K800 28021K800 28022K800 28099K800 28100K800 28101K800 28142K800 28143K800 28144K800 28145K800 28146K800 29191K800 29192K800 29193K800 29194K800 29195K800 29234K800 29235K800 29236K800 29293K800 29294K800 30300K800 30301K800 30322K800 30323K800 30338K800 30339K800 30356K800 30357K800 30358K800 30360K800 30361K800 30444K800 30446K800 30448K800 30450K800 30451K800 30452K800 31471K800 31472K800 31473K800 31474K800 32619K800 32620K800 32627K800 32628K800 32629K800 32630K800 32631K800 32632K800 32633K800 32680K800 32681K800 32682K800 33705K800 33709K800 33710K800 33711K800 33712K800 33713K800 33714K800 33715K800 33724K800 33735K800 33830K800 33831K800 34850K800 34850K801 34851K800 34858K810 34859K810 34862K800 34871K800 34872K800 34873K800 34874K800 34945K800 34946K800 34947K800 34948K800 34949K800 34950K800 35051K800 35052K800 35074K800 35075K800 35197K800 35976K800 35977K800 35978K800 36091K800 36093K800 36094K800 36096K800 36128K800 36129K800 36130K800 36131K800 36132K800 36133K800 37279K800 37279K801 37280K800 37281K800 37282K800 37322K800 37428K800 37429K800 25682SH00 27878SH00 28090SH00 29205SH00 29244SH00 31501SH00 32615SH00 32617SH00 34807SH00 34851SH00 36116SH00 26839SH00
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 Sensitive Infant Formula with Iron 7oz. can. 6 cans per case. 20.1oz. and 29.5oz. plastic jar. 4 jars per case. Item numbers: 68070 68072 68118 Retail UPCs: 070074680712 070074680736 070074681191

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-0947-2022
Lot/product code:
Batches: 30349SH00 30351SH00 30353SH00 32461SH00 36095SH00 34955SH00 34956SH00 34956SH01 34957SH00 36217SH00 32355K800 32464K800 35076K800 35077K800 36136K800 36137K800
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott EleCare Jr Amino Acid-Based Nutrition Powder Chocolate 14.1oz. can. 6 cans per case. Item numbers: 66273 Retail UPCs: 070074662718

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-0953-2022
Lot/product code:
Batches: 24532Z200 28129Z200 30400Z200 34935Z200 36154Z200
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 EleCare HMO, Abbott Similac EleCare, Abbott EleCare Similac Gold, Abbott EleCare Similac 400g can. 6 cans per case Item numbers: 6676006 6676012 6676021 6676025 6676030 6676045 6676053 6676057 Retail UPCs: 8699548995217 0070074124155 0070074123851 0070074120195 070074120850 070074122502 0070074120157

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-0929-2022
Lot/product code:
Batches: 25557Z200 27930Z200 28130Z201 29266Z200 30374Z200 30384Z201 32422Z201 33693Z200 36144Z202 25557Z201 30384Z202 33693Z202 34767Z201 35031Z202 36144Z205 27930Z202 36144Z203 25557Z203 30374Z202 36144Z204 34767Z202 25557Z205 28130Z200 29266Z201 30384Z200 32422Z202 33693Z201 35031Z201 36144Z200 25557Z204 28130Z202 30374Z201 32422Z210 34767Z200 35031Z200 36144Z201 25557Z202 27930Z201 28130Z203
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
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 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 Alimentum, Abbott Similac Alimentum, Abbott Similac Alimentum HMO, Abbott Alimentum Similac, Abbott Similac Gold Alimentum HMO 400g can. 6 cans per case. Item numbers: 674845 6748406 6748408 6748412 6748425 6748426 6748430 6748453 6748484 Retail UPCs: 0070074122250 8699548994869 070074122311 0070074124131 070074122359 070074122274 070074123349 070074123325

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-0936-2022
Lot/product code:
Batches: 33688Z201 34929Z202 35065Z201 36145Z202 29280Z260 32430Z200 36145Z201 28123Z262 33688Z202 23443Z261 25659Z260 30283Z260 31410Z200 31411Z201 32431Z200 25659Z261 28123Z261 30283Z262 31410Z204 25659Z262 26867Z262 28123Z263 29210Z202 30283Z263 33688Z203 35065Z202 29210Z201 33688Z204 23443Z260 25550Z260 25564Z260 26867Z260 27936Z260 27937Z260 28123Z260 29210Z200 29280Z261 30281Z260 30283Z261 31410Z201 31410Z205 31410Z206 31411Z200 32423Z200 32431Z201 33688Z200 34929Z200 35030Z200 35049Z200 35065Z200 35066Z260 36145Z200 25550Z261 26867Z261 32423Z201 32431Z202 34929Z201
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

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
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, LOW FAT YOGURT, FRUIT & GRANOLA PARFAIT, Newt, WT 9.oz , Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

Full report

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

Recall #:
F-0457-2023
Lot/product code:
UPC Code : 813141021090
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, Sausage Egg & Cheese Croissant Net Wt. 6.25 Oz. Single Serving, Mylar Wrap, Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

Full report

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

Recall #:
F-0456-2023
Lot/product code:
UPC Code : 813141020925
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, Strawberry Low Fat Yogurt, Fruit & Granola Parfait, Net Wt. 5.5 Oz. Single Serving, Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

Full report

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

Recall #:
F-0507-2023
Lot/product code:
UPC Code : 813141020826
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, Egg, Cheddar & Swiss Ciabatta, Net Wt. 5.3 Oz. Single Serving, Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

Full report

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

Recall #:
F-0477-2023
Lot/product code:
UPC Code : 813141020956
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 3, 2023

Bistro To Go, Turkey Sausage, Egg & Cheddar Muffin Net Wt. 5.5 Oz. Single Serving, Mylar Wrap, Keep refrigerated

On 02/03/2023, FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine of Baltimore, MD is initiating a recall of various products sold from January 24, 2023 through January 30, 2023 because the products have the potential to be contaminated with Listeria monocytogenes .

Full report

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

Recall #:
F-0455-2023
Lot/product code:
UPC Code : 813141022103
Recalling firm:
FRESH IDEATION FOOD GROUP, LLC dba Fresh Creative Cuisine
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)