Recall archive
31,892 recalls · page 20 of 1329
Reported Aug 5, 2026
GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IsoTis OrthoBiologics, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medical Action Industries, Inc. 306
FDA (openFDA device enforcement)
Reported Aug 5, 2026
EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp. UPC: 8 58792…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mellish Island Corp.
FDA (openFDA food enforcement)
Reported Aug 5, 2026
Dorzolamide HCl and Timolol Maleate Ophthalmic Solution, USP, 2%/0.5%, 10mL - bottle, Rx only, Manufactured by: Micro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro Labs USA Inc.
FDA (openFDA drug enforcement)
Reported Aug 5, 2026
Mycophenolate Mofetil for Injection USP, 500 mg/Vial, Single Dose Vial, 4 vials per carton, Rx only, Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mylan Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Aug 5, 2026
Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nelson & Isa Lacteos LLC
FDA (openFDA food enforcement)
Reported Aug 5, 2026Updated Sep 16, 2026
Immune Globulin (Human); Octagam IVIG 10% 30gm/300mL (Batch KP12B8561)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Octapharma Pharmazeutika Produktionsgesellschaft m.b.H.
FDA (weekly enforcement report)
Reported Aug 5, 2026Updated Sep 16, 2026
Proin ER, phenylpropanolamine hydrochloride extended-release tablets, 145mg Tablets, Net Contents 30 Tablets,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pegasus Laboratories, Inc.
FDA (weekly enforcement report)
Reported Aug 5, 2026
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Permobil Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker GmbH
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Power Over Fiber Base Module
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terex Utilities
FDA (openFDA device enforcement)
Reported Aug 5, 2026Updated Sep 16, 2026
Red Blood Cells, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Blood Center
FDA (weekly enforcement report)
DrugsReported Aug 5, 2026Updated Sep 17, 2026
Victory Medical Center Pharmacy recalls VMC Compounded Glutathione 200 mg/mL Multi-Dose Vials due to Elevated Endotoxin level
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Victory Medical Center Pharmacy
FDA (recalls & safety alerts)
Reported Aug 5, 2026
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Part Number AMS10411B; 2) ENT Pack,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026Updated Sep 16, 2026
EXO Black tattoo ink; 1FL.OZ & 8FL.Oz; packaged in black plastic individual containers. Use within 12 months of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xtreme Inks
FDA (weekly enforcement report)
FoodReported Aug 4, 2026Updated Sep 17, 2026
Blank Slate Creamery recalls Blank Slate Creamery Vegan Non-Dairy Frozen Dessert Coconut Fudge Sandwiches due to Undeclared egg allergen
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Blank Slate Creamery
FDA (recalls & safety alerts)
DrugsReported Aug 4, 2026Updated Sep 17, 2026
Liebel-Flarsheim Company, LLC recalls OPTIRAY OPTIRAY Imaging Bulk Package (IBP) 350, 500mL in vial (Ioversol Injection 74% 350 mg iodine/ml) due to Presence…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Liebel-Flarsheim Company, LLC
FDA (recalls & safety alerts)
Reported Aug 3, 2026
(Becton, Dickinson and Company) recalls BD Intraosseous Vascular Access System Needle Sets due to Due to Reports of Difficulty Removing the Obturator
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.(Becton, Dickinson and Company)
FDA (recalls & safety alerts)
DrugsReported Aug 3, 2026Updated Sep 17, 2026
American Regent, Inc. Animal Health recalls American Regent, Inc. Animal Health Adequan Canine Injection and Adequan i.m Injection for horses due to Visible…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.American Regent, Inc. Animal Health
FDA (recalls & safety alerts)
FoodReported Aug 3, 2026Updated Sep 17, 2026
Boticelli Foods recalls Bettergoods Pistachio Nut Butter due to Possible Salmonella Contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Boticelli Foods
FDA (recalls & safety alerts)
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