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Recalls affecting New Hampshire

Data last updated: September 7, 2026 at 2:36 PM UTC

16,277 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 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 EleCare Jr Amino Acid-Based Nutrition Powder Unflavored 14.1oz. can. 6 cans per case. Item numbers: 55253 Retail UPCs: 070074552545 70074552545

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-0951-2022
Lot/product code:
Batches: 23441Z200 25715Z200 26723Z200 26724Z200 26858Z200 27923Z200 27924Z200 27932Z200 27934Z200 29265Z200 30390Z200 30407Z200 31408Z200 34013Z200 34774Z200 35024Z200 35029Z200 36153Z200
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 Infant Formula with Iron 20.6oz. and 23.2oz. plastic jar. 4 jars per case; 34oz. plastic jar. 6 jars per case; 7oz. can. 6 cans per case. Item numbers: 66081 66655 67922 68088 Retail UPCs: 070074660806 070074666563 070074679167 070074680897

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-0931-2022
Lot/product code:
Batches: 23407SH00 23409SH00 24460SH00 24480SH00 24523SH00 24524SH00 25598SH00 25600SH00 25694SH00 25695SH00 25736SH00 25780SH00 26762SH00 26764SH00 26831SH00 26833SH00 27886SH10 23375SH00 23376SH00 23430SH00 23431SH00 24456SH00 24457SH00 24458SH00 24459SH00 24490SH00 24526SH00 24615Sh00 24615SH10 25570SH00 25586SH00 25652SH00 25653SH00 26749SH00 26750SH00 26752SH00 26759SH00 26761SH00 26824SH00 26825SH00 26826SH00 26827SH00 26828SH00 26829SH00 26841SH00 26843SH00 27881SH00 27882SH00 27883SH00 27884SH00 29181SH00 29182SH00 29225SH00 29226SH00 29228SH00 29295SH00 29296SH00 29297SH00 30308SH00 31457SH00 31459SH00 31460SH00 31462SH00 31483SH00 31484SH00 31486SH10 31488SH00 31490SH00 31492SH00 31493SH10 31493SH11 31494SH00 31550SH00 31551SH00 31577SH00 31578SH00 32616SH00 32618SH00 32668SH00 32669SH00 32670SH00 33736SH00 34798SH00 34960SH00 34961SH00 35039SH00 35040SH00 35041SH00 35042SH00 35198SH00 35962SH00 35963SH00 35964SH00 35965SH00 35966SH00 35967SH00 35968SH00 35969SH00 35970SH00 35971SH00 35972SH00 35973SH00 36189SH00 36190SH00 36191SH00 36193SH00 36194SH00 36195SH00 36196SH00 36219SH00 36220SH00 36221SH00 36222SH00 36223SH00 36224SH00 23401K800 23402K800 24479K800 25595K800 26842K800 27886K800 27957K800 27958K800 27959K800 27960K800 28012K800 28092K800 28103K800 28106K800 29185K800 30325K800 30326K800 30441K800 30441K810 30442K800 33717K800 33718K800 33779K800 33782K800 27974SH00 27975SH00 27976SH00 27991SH00 28008SH00 28010SH00 28104SH00 28105SH00 28156SH00 28157SH00 29206SH00 29222SH00 30305SH00 30306SH00 30307SH00 30340SH00 30341SH00 30342SH00 30362SH00 30363SH00 30369SH00 31481SH00 31482SH00 31573SH00 31575SH00 31576SH00 32590SH00 32591SH00 34810SH00 34812SH00 34812SH10 35060SH00 35061SH00 35082SH00 35082SH01 35083SH00 35084SH00 35990SH00 35991SH00 36134SH00 36135SH00 37292SH00 37293SH00
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
DrugChemicalRecalled February 16, 2022

Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5518-06

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-0209-2024
Lot/product code:
All lots, expiry on or before August 2023
Recalling firm:
TCP HRB ACQUISITON LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled February 16, 2022

Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5517-06

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-0208-2024
Lot/product code:
All lots, expiry on or before August 2023
Recalling firm:
TCP HRB ACQUISITON LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled February 16, 2022

Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged in a) 4 oz. (113g) aerosol cans (UPC 00827755070085, NDC 41595-7103-1) and b) 6 oz. (170g) aerosol cans (UPC 00827755070108, NDC 41595-7103-2), Distributed by Idelle Labs, Ltd. El Paso, TX 79912 USA

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-0207-2024
Lot/product code:
All lots, expiry on or before August 2023
Recalling firm:
TCP HRB ACQUISITON LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 30, 2021

Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles, Rx Only, Manufactured by Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-997-64

Stronger than it should be Drug

ALL 50 STATES
▸Full report

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

Recall #:
D-0295-2022
Lot/product code:
Lot #: 16345, Exp. Date 01/2024
Recalling firm:
Teligent Pharma, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 19, 2021

AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA Vitamin E & Moisturizer, 8 FL OZ (237 mL) bottle with either a black or clear top, Distributed by American Screening LLC Shreveport, LA, 71106 UPC 8 40050 51579 2

Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

ALL 50 STATES
▸Full report

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

Recall #:
D-0266-2022
Lot/product code:
Black capped bottles have no lot numbers but include expiration dates of 5/21/2022 and 05/24/2022. Clear capped bottles have neither lot numbers nor expiration dates.
Recalling firm:
American Screening LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 17, 2021

Enoxaparin Sodium Injection, USP, 40 mg/0.4 mL, Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Rx Only; 0.4 mL Syringes, Manufactured for Sandoz Inc., Princeton, NJ 08540, NDC 00781-3246-02; Carton (10 x 0.4 mL Syringes), Manufactured by Shenzhen Techdow Pharmaceutical Co., Ltd. Shenzhen City, Guangdong Province 518057, China for Sandoz Inc., Princeton, NJ 08540, NDC 00781-3246-64

Temperature Abuse; temperature excursion during shipping

ALL 50 STATES
▸Full report

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

Recall #:
D-0286-2022
Lot/product code:
Lot #SAB06761A, exp 04/2023
Recalling firm:
Sandoz Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 12, 2021

Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504

Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets

ALL 50 STATES
▸Full report

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

Recall #:
D-0092-2022
Lot/product code:
Lot #: 163935, Exp: 10/31/2022
Recalling firm:
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 18, 2021

X RATED HONEY FOR MEN, packaged in 15g packets, 4 packets per box, UPC 6 13682 41232 2

Marketed without an approved NDA/ANDA: Product found to be tainted with Tadalafil.

ALL 50 STATES
▸Full report

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

Recall #:
D-0819-2021
Lot/product code:
All lots, Exp. 12/2025
Recalling firm:
Phe Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 3, 2021

Lidocaine Hydrochloride Topical Solution, USP, 4% , 50 mL glass bottles, Rx Only, Teligent Pharma Inc. Buena, New Jersey 08310, NDC 52565-009-50.

Stronger than it should be Drug

ALL 50 STATES
▸Full report

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

Recall #:
D-0800-2021
Lot/product code:
Lot #:14218, Exp. Date 08/2022
Recalling firm:
Teligent Pharma, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 16, 2021

ALPHA MALE+ Male Enhancer, fruit chew strips, 1 strip per foil pouch, Distributed by Umbrella Labs, Made in the USA, UPC 8 60003 03770 6. Also manufactured for and distributed by: Alpha Male Plus, Tucson, AZ UPC 8 60003 74518 2 (pouch), UPC 8 60003 74512 0(carton)

Marketed Without an Approved NDA/ANDA: FDA analysis determined the presence of tadalafil

ALL 50 STATES
▸Full report

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

Recall #:
D-0001-2022
Lot/product code:
All lots within expiry
Recalling firm:
Alpha-Tek LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled July 14, 2021

Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 60+, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%) NET WT. 8.5 OZ. (240 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11255 6

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-0845-2021
Lot/product code:
06320E26, exp 1/2023
Recalling firm:
Johnson & Johnson Consumer, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled July 14, 2021

Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 50, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT. 6.5 OZ. (184 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11254 9

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-0844-2021
Lot/product code:
16621E01, exp 5/2024
Recalling firm:
Johnson & Johnson Consumer, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 14, 2021

Vy&Tea (Vietnamese Labeling with a green leaf and a bird underneath) 15/KLT 45.0G (15 tea sachets per box), Manufactured by Havyco No. 45, Group 1, National Highway 14, Son Hiep Hamlet, Tho Son Commune, Bu Dang District, Binh Phuoc Province, Vietnam, Website: trathaomocgiamcan.com.

Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine.

ALL 50 STATES
▸Full report

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

Recall #:
D-0749-2021
Lot/product code:
Best By Date: 9/2021
Recalling firm:
Qikmoov LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 22, 2021

Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont. 4 oz bottles, Manufactured in Dominican Republic: by Ardil Comercial S.R.L., Santo Domingo, Dominican Republic UPC 7 487040 301587

Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

ALL 50 STATES
▸Full report

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

Recall #:
D-0691-2021
Lot/product code:
Batch Number # 079932-4611-05-J, exp. date May 2022
Recalling firm:
Ardil Comercial S.R.L.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled May 12, 2021

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ / 250 mL bottle, Made in Mexico, Distributed by SBL Brands, LLC Las Vegas, NV 89119. UPC: 6 76753 00359 1

Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and 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-0781-2021
Lot/product code:
Lot No: E082020, "Best Buy": 5/21/2022
Recalling firm:
Global Sanitizers LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled May 12, 2021

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8 FL OZ (236 mL) bottle, Manufactured by Asiaticon, S.A. de C.V. Conkal 62, Jardines del Ajusco, Tlalpan, Ciudad de Mexico, C.P. 14200, Distributed by SBL Brands, LLC. Las Vegas, NV 89119. Made in Mexico UPC: 6 76753 00420 8,

Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and 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-0780-2021
Lot/product code:
Lot No: E082020, "Best Buy": 5/21/2022
Recalling firm:
Global Sanitizers LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 8, 2021

Ginseng Power 5000 capsule, 1- count per blister card, GS Natural Co, Los Angeles, CA 90010, UPC 0 40232 18144 3

Marketed without an approved NDA/ANDA: Products found to contain not listed on the label sildenafil and/ or tadalafil

ALL 50 STATES
▸Full report

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

Recall #:
D-0642-2021
Lot/product code:
all lots
Recalling firm:
NSNY Distributor Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 8, 2021

Premium OrgaZEN 7000 capsule, 1-count per blister card, distributed by: Nutra Vita Co, Santa Fe Springs, CA, Made in USA , UPC 0 40232 32555 7

Marketed without an approved NDA/ANDA: Products found to contain not listed on the label sildenafil and/ or tadalafil

ALL 50 STATES
▸Full report

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

Recall #:
D-0641-2021
Lot/product code:
all lots
Recalling firm:
NSNY Distributor Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

Thumbs Up 7 White 11K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil sildenafil, and vardenafil, FDA approved drugs making them an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.

ALL 50 STATES
▸Full report

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

Recall #:
D-0687-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil and sildenafil, two FDA approved drugs making it an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.

ALL 50 STATES
▸Full report

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

Recall #:
D-0688-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

Thumbs Up 7 Black 25K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil, an FDA approved drug making this an unapproved drug for which the safety and efficacy has not been established and therefore subject to recall.

ALL 50 STATES
▸Full report

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

Recall #:
D-0686-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)