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Recalls affecting Rhode Island

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

16,286 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 IIModerate risk
DrugRecalled June 23, 2022

GC MILK OF MAGNESIA CHERRY 12 FL OZ SKU 915000 GC MILK OF MAGNESIA MINT 12 FL OZ SKU 915623 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-1426-2022
Lot/product code:
SKUs: 915000; 915623
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

MIRALAX 8.3 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-1429-2022
Lot/product code:
SKU: 902219
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

BENADRYL EXTRA STRENGTH CREAM 1 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-1385-2022
Lot/product code:
SKU: 902163
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

DOCTOR DANDRUF 2N1 SHAMP CLN APL 13.5FLOZ SKU 2005726 SUAVE 2N1 MENS CC ANTI DNDRF SHMP 28 FLOZSKU 2006512 MANE N TAIL 2 IN 1 ANTI DANDRUFF 12 FL OZ SKU 2024652 HEAD AND SOULDERS 2N1 SMOOTH SILKY 12.8 FL OZ SKU 2097272 DOCTOR MED DANDRUFF TREAT 11 FL OZ SKU 2005531 HEAD AND SOULDERS CLASSIC CLEAN SH 13.5 OZ SKU 2099110 DOCTOR DANDRUF 2IN1 SHAM DRYSCLP 13.5FL OZ SKU 2038805 HEAD AND SOULDERS 2IN 1 DRY SCALP 13.5 FL OZ SKU 2038366 HEAD AND SOULDERS 2IN 1 DRY SCALP SHAMPOO 23.7 FLOZ SKU 2005504 DOCTOR DANDRUFF 2N1 SHAMPOO 13.5FL OZ SKU 2038806 DOCTOR SHAMPOO T GEL 8.5 FL OZ SKU 2038935 DOCTOR 2N1 DANDRUFF CLSC 23.7FLOZ SKU 2005121 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-1379-2022
Lot/product code:
SKUs: 2005726; 2006512; 2024652; 2097272; 2005531; 2099110; 2038805; 2038366; 2005504; 2038806; 2038935; 2005121
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 CTRZNE ALRGY ALL DY TBLT 5 CT SKU 900448 ZYRTEC CHILDRENS GRAPE 4 FL OZ SKU 999368 GOOD SENSE ALLERGY CETIRIZINE 10 MG TABLET 14 CT SKU 916897 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-1452-2022
Lot/product code:
SKUs: 900448; 999368; 916897
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

MUCINEX SE MAX STRENGTH 7CT 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-1460-2022
Lot/product code:
SKU: 900844
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

Hydrogen Peroxide 16 fl. oz. and 32 oz. bottles 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-1369-2022
Lot/product code:
SKUs: 909221, 901675
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 PAIN RELIEVER PM CAPLET 100 CT SKU 902381 GOOD SENSE PAIN RELIEVER APAP 500MG CAPLET 250CT SKU 902332 READY IN CASE PM PAIN RELIEVER CAPLET 50 CT SKU 913982 GOOD SENSE PAIN RELIEVER APAP ES 500 CT SKU 999029 GOOD SENSE PAIN RELIEVER CAPLET 100 CT SKU 913890 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-1392-2022
Lot/product code:
SKUs: 902381; 902332; 913982; 999029; 913890
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

LIDOCAINE ARTHRITIS AND SPORT WNTGRN 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-1389-2022
Lot/product code:
SKU: 902929
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

QP LAXATIVE BISACODYL 5 MG TABLET 50 CT SKU 902449 QP WOMEN LAXATIVE BISCODYL TABLET 25 CT SKU 915221 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-1425-2022
Lot/product code:
SKUs: 902449; 915221
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

SWAN CALAMINE LOTION 6 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-1411-2022
Lot/product code:
SKU: 901469
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

ST IVES BLKHD CLRNG GREEN TEA SCRUB 6 OZ SKU 2007787 AMBI EXFOLIATING WASH 5 OZ SKU 2097153 CC BLACKHEAD SCRUB 5 OZ SKU 2032021 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-1431-2022
Lot/product code:
SKUs: 2007787; 2097153; 2032021
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

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

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

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)
Class IIModerate risk
DrugRecalled June 23, 2022

MUCINEX FASTMAX CAPLETS COLD FLU 4CT 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-1457-2022
Lot/product code:
SKU: 903372
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

QP MOTION SICKNESS TABLET 8 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-1395-2022
Lot/product code:
SKU: 901583
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

DISNEY LICENSED ANTI BAC WIPES 20 CT SKU 998908; ANTIBACTERIAL WIPES 40CT SKU 2007538 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-1378-2022
Lot/product code:
SKUs: 998908; 2007538
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

BC ARTHRITIS PAIN FAST PAIN RELIEF 24CT SKU 999839 GOOD SENSE ARTHRITIS CAPLET 24 CT SKU 914771 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-1388-2022
Lot/product code:
SKUs: 999839; 914771
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

DR SCHOLLS CLR AWAY LIQ WART REMVR 20CT SKU 998384 DR SCHOLLS CALLUS REMOVER PADS 4CT SKU 998431 DR SCHOLLS CORN REMOVERS 9CT SKU 998403 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-1404-2022
Lot/product code:
SKUs: 998384; 998431; 998403
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

ROBITUSSIN COUGH N CHEST CONGESTION 4 FL OZ SKU 919471 DELSYM ORANGE 3 FL OZ SKU 901880 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-1453-2022
Lot/product code:
SKUs: 919471 ; 901880
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)