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Recalls affecting Montana

Data last updated: September 8, 2026 at 1:13 PM UTC

16,379 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 IIModerate risk
DrugRecalled June 23, 2022

ALKA SELTZER EXTRA STRENGTH 24 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1415-2022
Lot/product code:
SKU: 903323
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

AFRIN NO DRIP SEVERE CONGESTION 0.5FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1444-2022
Lot/product code:
SKU: 902045
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

RIC STOOL SOFTENER SOFTGEL 100 CT SKU 917000 RIC STOOL SOFTNER 100 CT SKU 902493 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1421-2022
Lot/product code:
SKUs: 917000; 902493
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

MYLICON INFANT GAS DROPS 0.5 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1442-2022
Lot/product code:
SKU:999109
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

VOLTAREN ARTHRITIS PAIN GEL 20G distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1434-2022
Lot/product code:
SKU: 998708
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

ACNE FREE ADAPALENE GL ACN TRTMT 0.5 OZ SKU 2096518 ACNE FREE TRMINTR 10 SPOT TRTMT 1 OZ SKU 2096507 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1433-2022
Lot/product code:
SKUs: 2096518; 2096507
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

GUARDIAN BISMUTH CHWBLE CHRY TABS 30 CTSKU 902321 RIC BISMUTH MAXIMUM STRENGTH 8 FL OZ SKU 914325 PEPTO BISMOL ORIGINAL 8 FL OZ SKU 914324 RIC BISMUTH REG STRENGTH CHERRY 8 FL OZ SKU 914781 PEPTO BISMOL CHERRY 8 FL OZ SKU 916063 PEPTO B LIQUID ORIGINAL TRAVEL 3.4 FL OZ SKU 999812 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1448-2022
Lot/product code:
SKUs: 902321; 914325; 914324; 914781; 916063; 999812
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

Novelty Hand Sanitizer with Silicone Wrap SKU 998890 Novelty Hand Sanitizer Assorted SKU 999330 Purell Hand Sanitizer Essentials 1 FL OZ SKU 2006819 Luxury Hand Sanitizer 16.9 FL OZ SKU 2007723 Suave Hand Sanitizer Lotion 3 FL OZ SKU 2096469 Purell Hand Sanitizer Original 6.5 FL OZ SKU 2095985 Purell Hand Sanitizer Soothing Aloe 6.5 Fluid Ounces SKU 2095986 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1363-2022
Lot/product code:
SKUs: 998890; 999330; 2006819; 2007723; 2096469; 2095985; 2095986
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

DIAL MENS EUCALYPTUS AB BODY WASH 20 FLOZ SKU 2096030 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1377-2022
Lot/product code:
SKU: 2096030
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

Orajel Cold Sore Pain Cream 1.25 fl. oz. distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1380-2022
Lot/product code:
SKU: 906766
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

BLISTEX LIP MEDEX 0.25OZ SKU 906120 BLISTEX LIP MEDEX POT 0.38 OZ SKU 998852 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1437-2022
Lot/product code:
SKUs: 906120; 998852
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

ALEVE ANALGESIC BACK MUSCLE 24 CT SKU 999787 ALEVE PM CAPLETS 20 CT SKU 900442 ALEVE CAPLET 50 CT SKU 916980 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1376-2022
Lot/product code:
SKUs: 999787; 900442; 916980
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

CARMEX DAILY CARE CHERRY SPF 15 0.35 OZ SKU 901842 CARMEX LIP BALM JAR 0.25OZ SKU 903284 CARMEX STRWBRRY STCK W SPF 15 0.15OZ SKU 905760 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1438-2022
Lot/product code:
SKUs: 901842; 903284; 905760
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

VASELINE ECZEMA CALMING THERPY CRM 6.8 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1413-2022
Lot/product code:
SKU: 2098741
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

JET ALERT TABLET 30 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1401-2022
Lot/product code:
SKU: 914001
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

ARTHRITIS HOT CREME 3 OZ SKU 901452 ICY HOT PATCH 1 CT SKU 911030 ICY HOT MUSCLE RUB 1.25 OZ SKU 920205 ICY HOT NO MESS 1.5 OZ SKU 998751 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1435-2022
Lot/product code:
SKUs: 901452; 911030; 920205; 998751
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

FLEET GLYCERIN SUPPOSITORIES 50 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1428-2022
Lot/product code:
SKU: 917001
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

Dermasil Dry Skin Treatment 10 OZ SKU 2098068 Aveeno Daily Moisturizing Lotion 5 OZ SKU 2005444 Aveeno Baby Daily Moistue Lotion 8 OZ SKU 900016 Vaseline Mens Extra Strength Body and Face Lotion 10 OZ SKU 2003674 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1366-2022
Lot/product code:
SKUs: 2098068, 2005444, 900016, 2003674
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

QP COUGH COLD TABLET 16 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1461-2022
Lot/product code:
SKU: 916922
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

VICKS VAPORUB 1.76 OZ SKU 919667 VICKS VAPOR RUB LAVENDER 1.76 OZ 999813 SWAN MEDICATED CHEST RUB 3.53 OZ SKU 920611 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1394-2022
Lot/product code:
SKUs: 919667; 999813; 920611
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

READY IN CASE RUBBING ALCHL 50 PCT WNTRGRN 16 FLOZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1390-2022
Lot/product code:
SKU:900535
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

COLGATE MAX FRESH CLEAN MINT 1.9OZ SKU 900596 COLGATE CAVITY PROTECTION 6OZ 3PK SKU 900734 SENSODYNE REPAIR AND PROTCT WHITNG 3.4 OZ SKU 901003 COLGATE BSPW PASTE BRISK MINT 6 OZ 2PK SKU 901658 COLGATE MAX FRESH COOL MINT 6OZ 2PK SKU 901785 COLGATE BSPW PASTE 6 OZ 3PK SKU 902143 CREST CMPLT SCOPE OUTLST PSTE 5.4OZ 2 PK SKU 902701 COLGATE TOTAL WHITENING TP 4.8 OZ SKU 902967 CREST 3D WHITE BRILLIANCE CHARCOAL 3.9 OZ SKU 903463 COLGATE BSPW GEL FROSTY MINT 6 OZ SKU 905026 ARM & HAMMER COMPLETE CARE BKS PRX TP 6 OZ SKU 905028 COLGATE BSPW PASTE BRISK MINT 2.5 OZ SKU 905703 COLGATE BSPW PASTE BRISK MINT 6 OZ SKU 907121 CREST BS N PX WHTE TUBE FRESH MINT 5.7 OZ SKU 907125 COLGATE SPARKLING WHITE MINT ZING 2.5 OZ SKU 907151 ARM & HAMMERADV WHITE TP 4.3 FL OZ SKU 907766 COLGATE MAX FRESH COOL MINT TP 6 OZ SKU 907839 CREST COMPLETE SCOPE OUTLAST TP 5.4 OZ SKU 907872 COLG MAX FRESH COOL MINT TP 6.3 OZ 3PK SKU 998200 COLGATE OW STAIN FIGHTR TOOTHPASTE 4.2 OZ SKU 998278 COLGATE MAX FRESH WHTNING CHRCOAL TP 6 OZ SKU 998881 COLGATE CHARCOAL TP 2.2 OZ SKU 998902 CREST 3D WHITE STAIN ERASER 3.1OZ TWN PK SKU 999286 COLGATE ESSENTIALS CHARCOAL PASTE 4.6 OZ SKU 999318 COLGATE TOTAL CLEANMINT TOOTHPASTE 4.8 OZ SKU 999498 COLGATE OW STAINFIGHTERCLEANMNT4.2OZ 2PK SKU 999633 COLGATE OW STAIN FIGHTER CLEAN MNT 4.2 OZ SKU 999750 COLGATE DEEP CLEAN GEL TOOTHPASTE 2.5 OZ SKU 999916 CREST TARTAR PROTECTION PASTE 5.7 OZ SKU 900353 COLGATE TOTAL WHITENING GEL 4.8OZ 2 PK SKU 903152 CREST CAVITY PROTECTION PASTE 5.7 OZ SKU 907327 CREST PRO HEALTH WHITENING GEL TP 4.6 OZ SKU 999760 AIM CAVITY PRTCT MINT GEL 4.5 OZ SKU 999910 CREST 3D WHITE RADIANT MINT 2.7 OZ SKU 907160 CR FRESH WHT PEP GIM 2.4 OZ SKU 900791 COLGATE SENSITIVE WHITENING PASTE 6 OZ SKU 901677 COLGATE TRIPLE ACTION 2.5 OZ SKU 907170 COLGATE OW STAIN PREVENTION TP 2.1 OZ SKU 998277 CREST 3D WHITE CHARCOAL 2.7 OZ SKU 999282 ARM & HAMMER PEROXICARE MINT PASTE 6 OZ SKU 999937 CREST ANTI CAVITY PASTE 2.4 OZ SKU 907165 CLOSE UP CINN RED GEL TP 4 OZ SKU 907220 COLGATE BSPW GEL TP 6OZ 3PK; SKU 902966 COLGATE TOTAL WHTN GEL TP 4.8 OZ SKU 906406 COLGATE CAVITY PROTECTION 6 OZ SKU 907329 COLGATE MAX FRSH ADV WHTN CLN MNT TP 6 OZ SKU 998257 CG OW SF MINT PASTE 2.0 OZ SKU 999723 COLGATE KIDS JUNIOR BUBBLE FRUIT 3.5 OZ SKU 900592 CREST BKING SDA PEROXIDE WHTNG TP 2.4 OZ SKU 907865 CREST KIDS SPRKL TPST 2.2 OZ SKU 901243 CREST 3D WHITE ARTIC FRESH 2.7 OZ SKU 905045 COLGATE RENEWAL GUM REVITALIZE TP 3 OZ SKU 998741 ULTRA BRITE ADV WHITENING TP 6 OZ SKU 902134 COLGATE BASE DEEP CLEAN GEL 6 OZ SKU 900728 COLGATE TOTAL WHTN PASTE TP 4.8OZ 2PK SKU 901784 SENSODYNE PRO NAMELGENTLE WHT 2.7 OZ SKU 902124 SWAN ULTRA CLEAN ARCTIC MINT 33.8 FL OZ SKU 902840 CREST 3DW ULTRA WHITE 3 OZ SKU 903453 COLGATE KIDS TP ASRTD CHARACTERS 4.6 OZ SKU 905517 PEPSODENT ORIGINAL TP 4.5 OZ SKU 907136 SENSODYNE EXTRA WHTEN TP 2.7 OZ SKU 907781 CREST PSTE DNSIFY DAILY WHITENING 4.1 OZ SKU 998268 ORAJEL PP FLUORIDE TOOTHPASTE 4.2 OZ SKU 998397 CREST 3D WHITE BRILLIANCE THPASTE 2.7 OZ SKU 998730 TOM'S KIDS STRAWBERRY ANTICAVITY 5.1 OZ SKU 999099 CREST 3D WHITE STNERSR ICY CLN MNT 3.1 OZ SKU 999285 SENSODYNE COMPLETE FRESH PASTE 3.4 OZ SKU 902363 CREST PRO HEALTH DEEP CLEAN TP 3.5 OZ SKU 903245 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1367-2022
Lot/product code:
SKUs: 900596, 900734, 901003, 901658, 901785, 902143, 902701, 902967, 903463, 905026, 905028, 905703, 907121, 907125, 907151, 907766, 907839, 907872, 998200, 998278, 998881, 998902, 999286, 999318, 999498, 999633, 999750, 999916, 900353, 903152, 907327, 999760, 999910, 907160, 900791, 901677, 907170, 998277, 999282, 999937, 907165, 907220, 902966, 906406, 907329, 998257, 999723, 900592, 907865, 901243, 905045, 998741, 902134, 900728, 901784, 902124, 902840, 905517, 907136, 907781, 998268, 998397, 998730, 999099, 999285, 902363, 903245, 903453
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

TN DICKINSON WITCH HAZEL 16 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1408-2022
Lot/product code:
SKU: 900911
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

ZZZQUIL NIGHT PAIN BERRY 12 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1400-2022
Lot/product code:
SKU: 903452
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

MY CHOICE LEVONORGESTREL TABLET distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

CGMP Deviations: product held outside appropriate storage temperature conditions.

ALL 50 STATES
Full report

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

Recall #:
D-1403-2022
Lot/product code:
SKU: 998211
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)