Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

3351–3375 of 5063

ModerateFDA (Drugs)·D-1392-2022·2022-08-31
Pain Reliever Caplets Recalled for Improper Storage Temperature
Over-the-counter pain reliever caplet products from Family Dollar stores are being recalled because they were stored outside proper temperature conditions.
Product
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
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1463-2022·2022-08-31
Maxim Instant Foam Hand Sanitizer recalled due to expired active ingredient
Midlab Incorporated is recalling Maxim Instant Foam Hand Sanitizer nationwide. The product was manufactured using expired benzalkonium chloride, potentially compromising effectiveness.
Product
Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303
Category
Drug
Distribution
0 states
ModerateFDA (Drugs)·D-1366-2022·2022-08-31
Personal Care Lotions Recalled Due to Improper Storage Temperature
Family Dollar Stores is recalling multiple lotion products that were held outside appropriate storage temperatures. The affected brands include Dermasil, Aveeno, and Vaseline products distributed from April 30 through June 10, 2022.
Product
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 thro
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1373-2022·2022-08-31
Multiple ibuprofen products recalled for improper storage temperature
Family Dollar is recalling multiple ibuprofen products, including MOTRIN and GOOD SENSE brands, due to improper storage temperature conditions at distribution facilities from April through June 2022.
Product
MOTRIN IB CAPLETS 24CT SKU999394; GOOD SENSE IBUPROFEN 200MG TABLETS 24CT SKU 900556;GOOD SENSE IBUPROFEN 200MG CAPLET 50 CT SKU 902333 MOTRIN CHILDREN'S BUBBLEGUM 4 FL OZ SKU 903048 GOOD SENSE IBUPROFEN REGULAR SOFTGELS 160CT SKU 999373 GOOD SENSE IBUPROFEN 200 MG CAPLE
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1412-2022·2022-08-31
Good Sense Sore Throat Spray Recalled for Improper Storage Conditions
Family Dollar Stores recalls Good Sense Sore Throat Spray Cherry 6 FL OZ due to CGMP deviations involving improper storage temperature conditions. The product was distributed nationwide from April 30, 2022 through June 10, 2022.
Product
GOOD SENSE SORE THROAT SPRAY CHERRY 6 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1449-2022·2022-08-31
Family Dollar Anti-Diarrheal Products Recalled for Improper Storage Conditions
Family Dollar Stores has recalled specific loperamide anti-diarrheal products distributed between April 30 and June 10, 2022, due to improper storage temperature conditions. Consumers should discontinue use and return affected products.
Product
GS ANTI DIARRHEAL LOPERAMIDE CAPLET 12 CT SKU 915632 IMODIUM AD MINT 4 OZ SKU 902080 IMODIUM AD CAPLET 6 CT SKU 915628 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1452-2022·2022-08-31
Three allergy medications recalled due to improper storage conditions
Family Dollar Stores is recalling three allergy medication products that were stored outside appropriate temperature ranges, violating Good Manufacturing Practice standards.
Product
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.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1382-2022·2022-08-31
Orajel Non Med Teething Gel Recalled for Improper Storage Conditions
Orajel Non Med Teething Gel 0.125 oz is being recalled by Family Dollar Stores due to products being held outside appropriate storage temperature conditions. No illnesses have been reported.
Product
ORAJEL NON MED TEETHING GEL 0.125 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1404-2022·2022-08-31
Dr. Scholls Wart and Callus Remover Products Recalled for Storage Deviation
Family Dollar Stores is recalling Dr. Scholls Clear Away Wart Remover, Callus Remover Pads, and Corn Removers distributed April 30 to June 10, 2022, due to improper storage conditions.
Product
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.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1424-2022·2022-08-31
Aspirin Products Recalled Due to Improper Storage Conditions at Family Dollar
Multiple aspirin products sold at Family Dollar Stores have been recalled due to storage temperature deviations during distribution from April 30 through June 10, 2022.
Product
FW ASPIRIN CHEWABLE TABLET 36CT SKU 913990 GS ENTERIC ASPIRIN TABLET 120 CT SKU 913724 BAYER BACK BODY EX STRGTH CAPLETS 24CT SKU 900438 BAYER LOW DOSE 81 MG TABLET 120 CT SKU 916070 BAYER ASPIRIN 325MG TABLET 24CT SKU 913996 BAYER LOW DOSE TABLET 32CT SKU 915641 BAYER
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1406-2022·2022-08-31
Baby Cough Medicine Recalled for Improper Storage Temperature
Zarbee's Naturals baby cough syrup has been recalled due to storage temperature deviations at Family Dollar stores between April and June 2022.
Product
ZARBEES NTRLS BABY CGH MUCUS GRP 2 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1439-2022·2022-08-31
MIDOL and Related OTC Menstrual Relief Products Recalled for Temperature Storage Deviation
Family Dollar Stores recalled MIDOL COMPLETE, QP MENSTRUAL RELIEF, and QP PMS FORMULA caplets distributed April–June 2022 due to CGMP deviations from improper storage temperature.
Product
MIDOL COMPLETE CAPLET 16 CT SKU 913028 QP MENSTRUAL RELIEF COMPLETE CAPLET 16CT SKU 999982 QP PMS FORMULA CAPLET 32 CT SKU 913232 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1379-2022·2022-08-31
Dandruff Shampoo Products Recalled for Improper Storage Temperature Conditions
Family Dollar Stores is recalling multiple dandruff shampoo brands sold between April and June 2022 because they were stored at improper temperatures. No illnesses have been reported.
Product
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
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1460-2022·2022-08-31
Mucinex SE Max Strength recalled for improper storage conditions
Family Dollar Stores is recalling Mucinex SE Max Strength 7CT distributed from April through June 2022 due to CGMP deviations involving improper storage temperature.
Product
MUCINEX SE MAX STRENGTH 7CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1441-2022·2022-08-31
Family Dollar Stye Eye Ointment Recalled Due to Improper Storage
Family Dollar is recalling Stye Eye Ointment 0.125 oz due to manufacturing deviations. The product was held outside appropriate storage temperature conditions.
Product
STYE EYE OINTMENT 0.125 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1395-2022·2022-08-31
QP Motion Sickness Tablet 8 CT Recalled for Improper Storage Conditions
Family Dollar Stores is recalling QP Motion Sickness Tablet 8 CT (SKU 901583) packages distributed nationwide from April 30 to June 10, 2022, due to improper storage temperature conditions.
Product
QP MOTION SICKNESS TABLET 8 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1411-2022·2022-08-31
Swan Calamine Lotion Nationwide Recall for Temperature Storage Deviations
Family Dollar Stores is recalling Swan Calamine Lotion 6 FL OZ due to CGMP deviations involving improper storage temperature. No illnesses or injuries have been reported.
Product
SWAN CALAMINE LOTION 6 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1451-2022·2022-08-31
CLARITIN Allergy Products Recalled Due to Improper Storage Conditions
Family Dollar Stores is recalling specific CLARITIN allergy products (liquids and tablets) distributed from April through June 2022 due to improper storage temperature conditions that may affect product quality.
Product
CLARITIN ALLERGY LIQ CHLDRNS GRAPE 2 FLOZ SKU 900834 CLARITIN ALLERGY 10MG TABLETS 5 CT SKU 916116 GS ALLERGY LORATADINE TABLET 30 CT SKU 916114 CLARITIN ALLERGY 10 MG TABLET 10 CT SKU 901655 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1377-2022·2022-08-31
Dial Men's Eucalyptus Body Wash Recalled Due to Storage Temperature Deviation
Family Dollar Stores is recalling Dial Men's Eucalyptus Body Wash 20 fl oz due to improper storage temperature conditions during distribution.
Product
DIAL MENS EUCALYPTUS AB BODY WASH 20 FLOZ SKU 2096030 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1461-2022·2022-08-31
QP Cough Cold Tablets Recalled for Improper Storage Conditions
QP Cough Cold Tablet 16 CT units distributed to specific Family Dollar Stores nationwide are being recalled due to storage temperature deviations. No illnesses or injuries have been reported.
Product
QP COUGH COLD TABLET 16 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1445-2022·2022-08-31
Nicorette Gum Recalled Due to Improper Storage Temperature Conditions
Family Dollar Stores is recalling NICORETTE GUM WHITE ICE MINT 4 MG distributed from April 30 through June 10, 2022. The product was held outside appropriate storage temperature conditions.
Product
NICORETTE GUM WHITE ICE MINT 4 MG 20 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1405-2022·2022-08-31
Zarbee's Natural Children's Cough + Mucus Syrup Recalled for Storage Temperature Deviations
Family Dollar Stores is recalling Zarbee's Natural Children's Cough + Mucus syrup distributed April through June 2022 due to CGMP violations involving improper storage temperature conditions that may compromise product quality.
Product
ZARBEES NTRL CHLD COUGH MUCUS GRP 4 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1459-2022·2022-08-31
QP Cold Multi-Symptom medication recalled for improper storage conditions
Family Dollar Stores is recalling QP Cold Multi-Symptom Day/Night medication distributed April 30–June 10, 2022, to select stores because the product was held at incorrect temperatures. Consumers should return the product to the store for a refund.
Product
QP COLD MULTI SYMPTM DAY NITE CPLT 24 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1380-2022·2022-08-31
Orajel Cold Sore Pain Cream Recalled for Improper Storage Conditions
Orajel Cold Sore Pain Cream 1.25 fl. oz. was recalled because it was stored outside appropriate temperature conditions. The product was distributed to Family Dollar Stores from April 30 through June 10, 2022.
Product
Orajel Cold Sore Pain Cream 1.25 fl. oz. distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1407-2022·2022-08-31
Good Sense Hemorrhoid Products Recalled for Improper Storage Conditions
Good Sense Hemorrhoid Ointment and Wipes sold at Family Dollar stores from April through June 2022 are being recalled due to storage outside appropriate temperature conditions. No illnesses have been reported.
Product
GOOD SENSE HEMORRHOID OINTMENT 2 OZ SKU 910325 GOOD SENSE HEMORRHOIDAL WIPES 48 CT SKU 902260 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide

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3351–3375 of 5063