Recall archive
31,892 recalls · page 65 of 1329
Consumer productsReported Mar 19, 2026
Tainoki Fine Furniture Recalls Office Chairs Due to Risk of Serious Injury and Fall Hazard
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Tainoki Fine Furniture
CPSC
Consumer productsReported Mar 19, 2026
Wagner Spray Tech Recalls 900 Series Power Steamers Due to Burn Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wagner Spray Tech Corp.
CPSC
Reported Mar 18, 2026
Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic streptococcal infection.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Altruan GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 capsules per bottle; Distributed by: Ambrosia Brands, LLC, 625…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ambrosia Brands LLC
FDA (openFDA food enforcement)
Reported Mar 18, 2026
DxC 700 AU, REF: B86444, B86446
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Mar 18, 2026
EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Secondary Packaging: STEAM NOODLES INGREDIENTS: ENRICHED FLOUR, WATER, STARCH, SALT, POTASSIUM, CARBONATE AND BENZOATE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CNC Noodle Corporation
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 18, 2026
Coco's Italian Market Heat-n-Eat Fettuccini Alfredo in homemade Alfredo Sauce, Net Wt. 19 oz. (510g), Keep Frozen,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cocos Wholesale and Imports, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 18, 2026
HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub
High riskUsing this product could cause serious injury, illness or death — stop using it now.House Of Flavors, Inc.
FDA (openFDA food enforcement)
Reported Mar 18, 2026
GEM Premier 5000 PAK, Part No. 00055360004.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory
19 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057
Moderate riskThis product could cause temporary or reversible health problems — stop using it.International Life Sciences
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
IBA Proton Therapy System - PROTEUS 235
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Mar 18, 2026
MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KOB GmbH
FDA (openFDA device enforcement)
Reported Mar 18, 2026
CLARITY II Laser System; Model No. 1110200210.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lutronic Corporation
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Made Fresh Salads brand Apple Cinnamon Cream Cheese; 5 lb white plastic tub
High riskUsing this product could cause serious injury, illness or death — stop using it now.Made Fresh Salads Inc.
13 more products in this recall
FDA (openFDA food enforcement)
FoodReported Mar 18, 2026Updated Sep 18, 2026
Mama Grande Tortilla Factory recalls Mama Grande Gorditas de Azucar and Doraditas de Azucar due to Undeclared Wheat and Soy
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Mama Grande Tortilla Factory
FDA (recalls & safety alerts)
Reported Mar 18, 2026
Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medartis AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
VEGETARIAN CHICKEN FLAVOR RAMEN Express Net wt 3oz (85g) Ingredients: Enriched unbleached flour (wheat flour***)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Palmetto Gourmet Foods Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 18, 2026
Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Penner Patient Care, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
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