Recall archive
31,892 recalls · page 142 of 1329
Consumer productsReported Jun 26, 2025
LED Fireplace Lanterns Recalled Due to Risk of Serious Injury or Death from Ingestion Hazard; Violations of Federal…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Green Pastures Wholesale
CPSC
Consumer productsReported Jun 26, 2025
Boyro Baby Walkers Recalled Due to Risk of Serious Injury or Death to Children from Fall Hazard; Violations of the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hangzhou Christine Trading Co. Ltd., dba Boyro Baby
CPSC
Consumer productsReported Jun 26, 2025
iHerb Recalls Bottles and Blister Packs of California Gold Nutrition Iron Supplements Due to Risk of Serious Injury or…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.iHerb LLC, dba Madre Labs LLC
CPSC
Consumer productsReported Jun 26, 2025
The Coleman Company Recalls Converta Camping Cots and Converta Camping Suspension Stretchers Due to Laceration and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Newell Brands Inc., an affiliate of The Coleman Company, Inc.
CPSC
Consumer productsReported Jun 26, 2025
DR Power Recalls Lithium-Ion Battery Packs Due to Fire and Burn Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ningbo New Team Import & Export Co. Ltd. ("Lera")
CPSC
Consumer productsReported Jun 26, 2025
Peg Perego Recalls Tatamia 3-in-1 Recliners, Swings and High Chairs Due to Risk of Suffocation; Violations of Multiple…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Peg Perego SPA
CPSC
Consumer productsReported Jun 26, 2025
Professional's Choice Sports Medicine Products Recalls Equine Bits Due to Fall Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Professional's Choice Sports Medicine Products Inc.
CPSC
Consumer productsReported Jun 26, 2025
Sanven Technology Recalls Vevor Handrails Due to Injury Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sanven Technology Ltd., dba Vevor
CPSC
Consumer productsReported Jun 26, 2025
Total Saddle Fit Recalls Western Saddle Cinches Due to Fall and Injury Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Total Saddle Fit, LLC
CPSC
Reported Jun 25, 2025
AFGHANI CORN BREAD "Doda"; INGREDIENTS: Corn Flour, Sugar, Vegetable Oil, Eggs, Milk, Black Seeds, Caardamom; ALLERGEN…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ariana Sweets Inc.
FDA (openFDA food enforcement)
Reported Jun 25, 2025
Acetaminophen Tablets, 325 mg, 100-count bottles, Distributed by: Amazon.com Services LLC, 410 Terry Avenue N.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aurobindo Pharma USA Inc.
FDA (openFDA drug enforcement)
Reported Jun 25, 2025
CPK TEQUILA LIME BASE ALLERGENS: MILK NET WEIGHT: 1 LB Case UPC FG15453558 Manufactured for California Pizza Kitchen,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bakkavor Foods USA, Inc.
FDA (openFDA food enforcement)
Reported Jun 25, 2025
Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Balt USA, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Big Y various sandwiches made to order at deli counter (Subs (small, large, supersub), wrap, panini, grinders); UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Big Y Supermarkets
FDA (openFDA food enforcement)
Reported Jun 25, 2025
SURGIMESH WN, Polymeric Surgical Mesh, Large Flat Sheet, Model/Catalog Number: T3030
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chamberlain Technologies LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Incorporated
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dexcom, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2025
STA - Owren Koller. Model/Catalog Number: 00360 STA - Owren-Koller is a buffer solution intended for use as a diluent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Gentamicin Injection, USP, (PEDIATRIC), 20 mg per 2 mL (10 mg per mL*), 2 mL Single-Dose Vial, Rx Only, Mfd. in India…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eugia US LLC
FDA (openFDA drug enforcement)
Reported Jun 25, 2025
5008X HDF Hemodialysis Blood Tubing Set, 24 units per case, with the following models: a. 5008X Standard HDF Bloodline,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Jun 25, 2025
Cucumber Bowl with Ranch dip 15oz UPC 850054894519 Purchase Dates: 05/08/2025 to 05/21/2025 Cucumber Slices W/Tajin 10…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GBC Food Services, LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 25, 2025
Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device Model/Catalog Number: PM001 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Guangzhou Pluslife Biotech Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 25, 2025
AcoSound. Model Number: LW12-BTE-M
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hangzhou Acosound Technology Co., Ltd.
FDA (openFDA device enforcement)
Reported Jun 25, 2025
ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001 , and 3) 400021003; infusion pump
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
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