Recall archive
31,892 recalls · page 39 of 1329
Consumer productsReported Jun 11, 2026
Nimood Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation…
High riskUsing this product could cause serious injury, illness or death — stop using it now.shenzhenshinikezhinengshebeiyouxiangongsi (Shenzhen Nike Intelligent Equipment Co., Ltd.) dba Nimood US
CPSC
Consumer productsReported Jun 11, 2026
Arctic Zone Titan Pro Coolers Recalled Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Black Sheep Fam
CPSC
FoodReported Jun 11, 2026Updated Sep 17, 2026
Total Nutrition Inc. recalls TNVitamins and Doctor’s Pride TNVitamins Ultra Potent Complete Green Superfood Capsules and Doctor’s Pride Complete Green…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Total Nutrition Inc.
FDA (recalls & safety alerts)
Consumer productsReported Jun 11, 2026
Yamaha Recalls Model Year 2021-2022 Fleet Golf Cars Due to Risk of Serious Injury or Death from a Crash Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Yamaha Golf-Car Company
CPSC
Consumer productsReported Jun 11, 2026
Yamaha Recalls UMAX Bistro and Bistro Deluxe Vehicles Due to Injury Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Yamaha Golf-Car Company
CPSC
Reported Jun 10, 2026
Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid Scala Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Bionics, LLC
FDA (openFDA device enforcement)
Reported Jun 10, 2026
UPC 22655200000 CAKE CARROT 8IN 2-Layer UPC 27813200000 CAKE CARROT 8IN 2-Layer These are Albertson's store-made items…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Albertsons Companies LLC
120 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 10, 2026
Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, Rx Only, 30-count bottle, Manufactured by: Alkem Laboratories…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories, LLC
FDA (openFDA drug enforcement)
Reported Jun 10, 2026
Duloxetine DR Capsules, 30 mg, 30 count bottles, Rx, Relabeled by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Asclemed USA Inc.
FDA (openFDA drug enforcement)
Reported Jun 10, 2026
Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
BD Pyxis MedStation 4000 REF: 303 Medication cabinet
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code: 60884522007028 The devices are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Betaine Anhydrous, 2055kg, material packed in foil bags inside 15kg cardboard box Label reads in part as "***BETAINE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Creative Compounds, LLC
FDA (openFDA food enforcement)
Reported Jun 10, 2026
Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Daavlin Distributing Company
FDA (openFDA device enforcement)
Reported Jun 10, 2026
DeRoyal Industries Inc. Ref 46-406, Covaderm Plus, Vascular Access Dressing 6"x6" (15cmx15cm)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Atlan A350. Model Number: 8211500. anesthesia workstation
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Eugia US LLC
FDA (openFDA drug enforcement)
Reported Jun 10, 2026
LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresenius Kabi USA, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2026
MAC 5 A4 Resting ECG Analysis System 855001-001; MAC 5 A5 Resting ECG Analysis System 8855002-001. Electrocardiograph
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems China Co., Ltd.
FDA (openFDA device enforcement)
Reported Jun 10, 2026
CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Information Technologies Inc.
FDA (openFDA device enforcement)
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