Recall archive
31,892 recalls · page 119 of 1329
Reported Sep 17, 2025
Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AVID Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 17, 2025
chloroproMAZINE Hydrochloride Tablets, USP, 50 mg, 50 Tablets (5x10) unit dose carton, Rx only, Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AvKARE
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 17, 2025
Brand Name: CELSITE Product Name: CELSITE BABYPORT SET PUR 4,5F IV USA Model/Catalog Number: 5433742 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B.Braun Medical S.A.S.
FDA (openFDA device enforcement)
Reported Sep 17, 2025
Boston Scientific Encore 26 Inflation Device, Material Numbers (UPN): 1. H74904526011; 2. H74904526052; 3. M0067101140;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 17, 2025
Duloxetine Delayed-Release Capsules, USP, 30 mg, 1,000 Capsules per bottle, Rx Only, Manufactured by: Towa…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breckenridge Pharmaceutical, Inc.
FDA (openFDA drug enforcement)
Reported Sep 17, 2025
Brand Name: Fortress Introducer Sheath System Product Name: Fortress Introducer Sheath System Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contract Medical International GmbH
FDA (openFDA device enforcement)
Reported Sep 17, 2025
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x 100 um, SterileEO, RX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Corneat Vision, Ltd.
FDA (openFDA device enforcement)
Reported Sep 17, 2025
Anabolic Research WINN-50 (vanazolol). Dietary Supplement. 90 Capsules. UPC 8 51840-00707 6. Manafactured For: Anabolic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dynamic Sports Nutrition
FDA (openFDA food enforcement)
Reported Sep 17, 2025
Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 17, 2025
4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10 mL (0.5 mEq/mL), For Intravenous Use Only, 10 mL Single Dose Vial, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exela Pharma Sciences LLC
FDA (openFDA drug enforcement)
Reported Sep 17, 2025
Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen, Zinc Oxide 22.75%, a) 15 mL, 0.5 fl. oz. per tube,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Grace & Fire Pty Ltd.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 17, 2025
Haifa Smoked Fish recalls Haifa Cold Smoked Salmon and Cold Smoked Seabass due to Potential contamination with Listeria monocytogenes
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Haifa Smoked Fish
FDA (recalls & safety alerts)
Reported Sep 17, 2025
Hershey s Ice Cream, Green Mint Chip (GMC) Bulk, 3 gallons, 1 unit , bulk can- a cardboard tub with metal rings and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hershey Creamery Co.
FDA (openFDA food enforcement)
Reported Sep 17, 2025
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, 10mg,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lannett Company Inc.
FDA (openFDA drug enforcement)
Reported Sep 17, 2025
Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.M.O.M Enterprises, LLC.
FDA (openFDA food enforcement)
Reported Sep 17, 2025
10Fore Hemostasis Valve Catalog Number / UDI-DI code: MAPTEN4 / 00884450821305 MAPTEN42 / 00884450832509 MAPTEN452 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Sep 17, 2025
NOxBOXi Nitric Oxide Delivery System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noxbox Ltd.
FDA (openFDA device enforcement)
Reported Sep 17, 2025
ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019. The ViziShot 2 FLEX tissue biopsy device is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Sep 17, 2025
TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degree, 45 degree and 60 degree.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Omnia Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 17, 2025
PILLAR SA Ti, STERILE, 37mm (W) x 28mm (D) x 18mm (H), 20-degrees, REF: 82-3713SP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix U.S. LLC
FDA (openFDA device enforcement)
Reported Sep 17, 2025
IntelliSpace Cardiovascular, Software 8.0.0.4.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.V.
FDA (openFDA device enforcement)
Reported Sep 17, 2025
Brand Name: ReQuest Measles IgM Product Name: Enzyme Linked Immunoabsorbant Assay, Rubeola IgM Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quest International, Inc.
FDA (openFDA device enforcement)
Reported Sep 17, 2025
QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Sep 17, 2025
Ciprofloxacin 0.3% and Dexamethasone 0.1% Otic Suspension Rx Only, For Use in Ears Only, Manufactured By: Novartis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz Inc.
FDA (openFDA drug enforcement)
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