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Recalls affecting New York

Data last updated: September 9, 2026 at 1:18 PM UTC

17,381 recalls found
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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/virusSalmonellaAnnounced 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/virusE. coliAnnounced 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)
UnclassifiedAllergenMilkUndeclaredAnnounced 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)
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)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced 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/virusSalmonellaAnnounced 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)
Wording
Class IIModerate risk
DrugRecalled June 23, 2022

BANANA BOAT SPRT CLR SPRY SPF50 6 FL OZ SKU 2007524 SUNTONE SPORT SPRAY SPF 50 5.5 OZ SKU 2096102 HAWAIIAN TROPIC TANNING OIL SPRAY PUMP SPF 25 8 FL OZ SKU 2096111 BANANA BOAT SPORT ULTRAMIST SPRAY SPF 65 6 OZ SKU 2096117 COPPERTONE WATERBABIES LOTION SPF 50 8 FL OZ SKU 2097635 COPPERTONE SPORT SPRAY SPF 50 5.5 OZ SKU 2097636 BANANA BOAT SPRT LTION SPF 50 8 FL OZ SKU 2099592 HAWAIIAN TROPIC SHEER TOUCH LOTION SPF 30 8 FL OZ SKU 2006432 BB KIDS SUN SCREEN MIST SPRAY SPF 100 6 OZ SKU 2007523 SUNTONE KIDS SPRAY SPF 50 6 OZ SKU 2096096 NEUTROGENA BCH DFNSE SPR SPF 70 SKU 2097632 BANANA BOAT KDS SPRT SPRY SPF50 6FL OZ SKU 2097655 BANANA BOAT DRY OIL MST SPRY 15 SPF 6 OZ SKU 2097794 BANANA BOAT TAN DRY OIL MIST 4 SPF 6 OZ SKU 2097144 COPPERTONE GLOW SPRAY SPF 50 5OZ SKU 2096124 COPPERTONE SPORT LOTION SPF 50 8.75 FLOZ SKU 2096130 NEUTROGENA ULTRA SHEER LOTN SPF 55 3 FL OZ SKU 2097637 SUNTONE KIDS LOTION SPF 50 6 FL OZ SKU 2096101 BANANA BOAT SPORT ULTRA MIST 30 SPF 6 OZ SKU 2097141 COPPERTONE SPORT SPRAY SPF30 5.5OZ SKU 2097083 SUNTONE SPORT SPRAY SPF 70 5.5 OZ SKU 2008234 SUNTONE SPORT LOTION SPF 50 6 FL OZ SKU 2096099 COPPERTONE KIDS SPRAY SPF 50 5.5 OZ SKU 2097084 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-1365-2022
Lot/product code:
SKUs: 2007524, 2096102, 2096111, 2096117, 2097635, 2097636, 2099592, 2007523, 2096096, 2097632, 2097655, 2097794, 2097144, 2096124, 2096130, 2097637, 2096101, 2097141, 2097083, 2008234, 2096099, 2097084; 2006432
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

VICKS VAPOCOOL DROPS SEVERE 18 CT SKU 999488 BEST HEALTH HONEY LEMON COUGH DROP 80 CT SKU 998844 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-1399-2022
Lot/product code:
SKUs: 999488; 998844
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

DR SCHOLLS ANTI FUNGAL SPRAY PWDER 4.7 OZ SKU 998250 PREMIER ANTFGL TLNFTT LQ SPRY 5.3 FL OZ SKU 911077 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-1375-2022
Lot/product code:
SKUs: 998250; 911077
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

MEDIC EYE DROPS MAX REDNESS SKU 998920 CLR EYS MX RDNS RLIF 0.5 FL OZ SKU 901844 SYSTANE ULTRA HIGH PRFRM LUB DRPS 0.14 FLOZ SKU 901961 LUMIFY REDNESS REL EYE DROPS 2.5 FL OZ SKU 998300 FC EYE DROPS ADVANCED 0.5 OZ SKU 902280 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-1430-2022
Lot/product code:
SKUs: 998920; 901844; 901961; 998300; 902280
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

PEPCID COMPLETE CHEWABLE TAB BERRY 8CT SKU 903365 PEPCID AC MAXIMUM STRENGTH TABLET 25 CT SKU 902063 PEPCID AC MAXIMUM STRENGTH TABLET 8 CT SKU 914773 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-1419-2022
Lot/product code:
SKUs: 903365; 902063; 914773
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

JOHNSONS BABY FIRST TOUCH GIFT SET 4PC 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-1447-2022
Lot/product code:
SKU: 999553
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

REFENESEN MUCUS RELIEF TABLET 30 CT SKU 917531 MUCINEX DM MAX STRENGTH 7CT SKU 900854 RIC MUCUS RLF DM MAX STNGTH CHRY 6FL OZ SKU 999559 VICKS JARABE COUGH CONGESTION 8FLOZ SKU 998933 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-1456-2022
Lot/product code:
SKUs: 917531; 900854; 999559; 998933
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

SUAVE INV SLD PWDR 1.2 OZ SKU2004504 SUAVE AP INV SOLID SWEET PEA 1.2 OZ SKU 2004622 LADY SPEED STICK AP WILD FREESSIA 1.4OZ SKU 2005184 SUAVE AP DEOD POWDER 2.6 OZ 2PK SKU 2028126 SCRT IN SLD PWDR FRSH 2.1OZ 2PK SKU 2028363 LADY SPD STK AP INV PWDR 1.4OZ SKU 2028365 DEGREE INV SLD XBLST 2.7 OZ 2PK SKU 2028378 SECRET DEO INV SHWR FRSH 2.1 OZ SKU 2028538 SUAVE DEO TRPCL PARADISE 1.2 OZ SKU 2028544 SECRET DS WHTE PECH ARGN OIL SPRY 4.1 OZ SKU 2095889 SECRET DS WILD ROSE OIL SPRAY 4.1 OZ SKU 2095896 DOVE ADVANCED COOL ESSENTIALS 2.6OZ SKU 2099968 OLD SPICE RED ZONE DEO SWAGGER 3OZ SKU 2005168 OLD SPICE HE FRESH DEO 2.4OZ 2PK SKU 2007730 SECRET OUTLAST CLEAN LVNDR GEL 2.6OZ SKU 2098900 OLD SPICE WC IS BEARGLOVE 2.6OZ SKU 2099254 DEGREE FMAL BLCK WHT PURERN DRYSPRY3.8OZ SKU 2003471 DEGREE EXTREME BLAST IS 2.7 OZ SKU 2005214 SECRET FRESH IS COCOA BUTTER 2.6OZ SKU 2007898 SECRET OUTLAST IS COMPLETELY CLEAN 2.6OZ SKU 2001333 DEGREE ML INVIS SLD COOL RUSH 1.7OZ SKU 2002557 OLD SPICE RZ SWAGGER 2.6 OZ SKU 2004512 DOVE AP INV SLD FRESH 1.6 OZ SKU 2028253 DEGREE FOR WOMEN IS BW PURE RAIN 2.6 OZ SKU 2096622 DEGREE BLCK WHIT PURE CLN DRY SPRY 3.8 OZ SKU 2003471 DEGREE MEN INV SLD SPORT TWIN 2.7 OZ 2PK SKU 2001309 SECRET INVS SLD PWDR FRSH 2.1 OZ SKU 2028310 DOVE ADVANCED CARE IS COCONUT 2.6 OZ SKU 2006902 SECRET FRESH EXP PARIS ROSE GEL 2.6 OZ SKU 2098479 OLD SPICE FIJI 2.6OZ SKU 2001336 SECRET AP STICK FRSH PWD 1.7OZ SKU 2028566 DOVE MEN AP INV SLD XTRA FRSH 2.7 OZ SKU SECRET OUTLAST CLR GEL PWDR PROTEC 2.6OZ SKU 2044343 DOVE CARING COCONUT DRY SPRAY 3.8OZ SKU 2097527 DOVE CLR FNSH 100 CLRS DRY SPR 3.8FLOZ SKU 2098905 AXE AP INV SLD DK TEMPT 2.7OZ SKU 2028222 DOVE DRY SPRAY COOL ESSENTIALS 3.8 OZ L2 SKU 2006098 DEGREE FMLE INV SLD TWN PWDR 2.6 OZ 2PK SKU 2001311 OLD SPICE HE PLAYMAKER 2.4 OZ SKU 2004835 GIL CLEAR GEL COOL WAVE 2.85 OZ 2PK SKU 2005220 DEGREE WMNS SEXY INTRIGUE 2.6 OZ SKU 2028194 MENNEN SPEED STCK AP INV SLD FRSH 1.8 OZ SKU 2028249 DOVE INV SLD POWDER 1.6 OZ SKU 2028255 DEGREE AP INV SLD XBLAST 1.7 OZ SKU 2028257 AH ULTRAMAX INV SLD FRSH SCT 1 OZ SKU 2028315 POWER STICK LADY AP POWDER FRESH 1.7 OZ SKU 2044190 DOVE MENS INV SOLID CLEAN COMFORT 1.7 OZ SKU 2097528 AXE APOLLO INV SOLID DEODORANT 1.7 OZ SKU 2097534 DEGREE AP INV SLD FRESH 2.6OZ SKU 2028218 SUAVE AP INV SLD TRPCL PARDSE 2.6 OZ SKU 2004752 DEGREE AP INV SLD SHOWR 1.6 OZ SKU 2028258 SUAVE MENS ACTIVE SPORT 2.7OZ SKU 2098472 OLD SPICE INV SLD KRAKENGARD 2.6OZ SKU 2098901 AXE ANARCHY INVISIBLE SOLID 2.7 OZ SKU 2005211 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-1370-2022
Lot/product code:
SKUs: 2098901; 2005211; 2004504; 2004622; 2005184; 2028126; 2028363; 2028365; 2028378; 2028538; 2028544; 2095889; 2095896; 2099968; 2005168; 2007730; 2098900; 2099254; 2003472; 2005214; 2007898; 2001333; 2002557; 2004512; 2028253; 2096622; 2003471; 2001309; 2028310; 2006902; 2098479; 2001336; 2028566 ; 2004735 ; 2044343 ; 2097527 ; 2098905 ; 2028222 ; 2006098 ; 2001311 ; 2004835 ; 2005220 ; 2028194 ; 2028249 ; 2028255 ; 2028257 ; 2028315 ; 2044190 ; 2097528 ; 2097534 ; 2028218 ; 2004752 ; 2028258; 2098472
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

DULCOLAX 5 MG TABLET 25 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-1427-2022
Lot/product code:
SKU: 916079
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

NPX TRIPLE ANTIBIOTIC OINTMENT 1 OZ SKU 910320 NPX PAIN ITCH SCAR ANTIBAC OINTMENT 1 OZ SKU 999855 NPX TRPL ANTIBIOTIC PLS PAIN OINMNT 1 OZ SKU 901498 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-1383-2022
Lot/product code:
SKUs: 910320; 999855; 901498
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

SWAN POVIDONE 4 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-1410-2022
Lot/product code:
SKU: 999843
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

ZARBEES NTRL CHLD COUGH MUCUS GRP 4 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-1405-2022
Lot/product code:
SKU: 999983
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

FS HYDROCORTISONE CREAM 1 OZ SKU 910321 CORTIZONE 10 CREME 0.5 OZ SKU 910167 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-1384-2022
Lot/product code:
SKUs: 910321; 910167
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

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

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

EXCEDRIN MIGRAINE CAPLET 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-1446-2022
Lot/product code:
SKU: 913722
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

GUARDIAN ANTACID EX STRGTH TBLT FRT 96CT SKU 901379 GUARDIAN CHWABLE SMTHIES BRRY FSION 60CT SKU 999845 GS EFFERVESCENT ANTACID TABLET 36 CT SKU 913102 GUARDIAN ANTCD TBLT XTRA STGTH BRY 96 CT SKU 914109 GUARDIAN ANTCID TBLT REG STTH FRT 150 CT SKU 914726 GC ANTACID SUPREME CHERRY 12 FL OZ SKU 914112 GUARDIAN ANTD ULTR STRGTH 1000 FRT 72 CT SKU 902322 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
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A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1414-2022
Lot/product code:
SKUs: 901379; 999845; 913102; 914109; 914726; 914112; 902322
Recalling firm:
Family Dollar Stores, Llc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled June 23, 2022

STYE EYE OINTMENT 0.125 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
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A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1441-2022
Lot/product code:
SKU: 998301
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)