Recall archive
31,892 recalls · page 108 of 1329
Reported Oct 22, 2025
Fasenra (benralizumab) Injection, 30 mg/mL, one single-dose pre-filled syringe, Rx only, Manufactured by: AstraZeneca…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Astrazeneca Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Oct 22, 2025
CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
15 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2025
BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic heads Part ID/Description: 18593 HEAD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioPro, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Free Range Grade A Large Brown Eggs, 12ct Cartons, UPC: 860010568507, Black Sheep Egg Company 400 S Memorial Drive…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Black Sheep Egg Company, LLC
9 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 22, 2025
ACCOLADE SR SL (Model L300)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
33 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated Embolic Protection (Neuroguard IEP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Contego Medical LLC
FDA (openFDA device enforcement)
Reported Oct 22, 2025
DuoDERM" Extra Thin dressings are highly flexible, control gel formula dressings designed for use on dry to lightly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Zenith Alpha 2 Thoracic Endovascular Graft, Catalog Prefix ZTA2- Reference Part Numbers ZTA2-P-40-117-W ZTA2-P-40-167…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Medical Incorporated
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Haifa COLD SMOKED SALMON 8 OZ.
High riskUsing this product could cause serious injury, illness or death — stop using it now.D & M Smoked Fish, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 22, 2025
Product: STA Liatest D-Di; REF: 00515;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Wegmans Ultimate Plain Cheesecake Large Net Wt 3.13 lb (1.42kg), shrink wrapped in a collar, 8 cakes per wholesale case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eli's Cheesecake Company
FDA (openFDA food enforcement)
Reported Oct 22, 2025
Everolimus tablets 5mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Endo USA, Inc.
FDA (openFDA drug enforcement)
Reported Oct 22, 2025
ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Oct 22, 2025
FERNO POWER X2 POWERED AMBULANCE COT, Model/Catalog Number: 0015816; FOR USE IN GROUND TRANSPORTATION AMBULANCES.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used with Disinfection Kit User Manual, REF: UI-185043723
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fisher & Paykel Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Sliced (1/4") green onions, refrigerated, packaged in plastic bag. Each case consist 5/6lbs. bag (net wt. 30lbs.).…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Garden Fresh Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 22, 2025
LOGIQ P10 series with software version R4.5.7 Model Number 5877534
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Viorele, Desogestrel and Ethinyl Estradiol, USP, 0.15 mg/ 0.02 mg and Ethinyl Estradiol Tablets, USP, 0.01 mg, 3…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Glenmark Pharmaceuticals Inc., USA
FDA (openFDA drug enforcement)
Reported Oct 22, 2025
1. SILVER HORSE - PURE ALUMINIUM MADE IN INDIA - ALUMINIUM MILK PAN 4 inches 2. SILVER HORSE - ALUMINIUM MATHAR KADAI -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Goyal Group Inc.
FDA (openFDA food enforcement)
Reported Oct 22, 2025
Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300. Product Description: The CycloPen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Iantrek Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 22, 2025
The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Insulet Corporation
FDA (openFDA device enforcement)
Reported Oct 22, 2025
Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.IntegraDose Compounding Services LLC
FDA (openFDA drug enforcement)
Reported Oct 22, 2025
Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kico Knee Innovation Company
FDA (openFDA device enforcement)
Reported Oct 22, 2025
XERF EFFECTOR 60. Electrosurgical unit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lutronic Corporation
FDA (openFDA device enforcement)
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