Recall archive
31,892 recalls · page 87 of 1329
Reported Dec 24, 2025
1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Copan Italia
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Cardiosave Hybrid
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Datascope Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Intelerad InteleShare software, with ProViewer component
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DICOM Grid, Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Linzer Hearts Baked Cut Out Cookies UPC 0 44964 22072 2 72 - 4.0 oz Cut Cookies CBB-220-LZ Net Weight: 18 lbs…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dough-To-Go Inc.
FDA (openFDA food enforcement)
Reported Dec 24, 2025
Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant Model/Catalog Numbers: 600-601 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dsaart LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Software for the controlled administration of fluids to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresenius Kabi USA, LLC
FDA (openFDA device enforcement)
Reported Dec 24, 2025
5008X CAREsystem +CLiC +CDX;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2025
GE HealthCare ViewPoint 6, Catalog Number H47601AA; Radiological image processing system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare GmbH
FDA (openFDA device enforcement)
Reported Dec 24, 2025
GE Healthcare Carestation anesthesia system, product number and REF numbers: Carestation 610 A1, REF 1012-9620-222;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Medical Systems China Co., Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Medical Supply Inc.
FDA (openFDA drug enforcement)
Reported Dec 24, 2025
BaiLiFeng Dried Cinnamon Powder; Net Wt 4 oz/114G; Good Way Trading Group Inc 58-51 Maspeth Avenue Maspeth NY 11378;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Good Way Trading Group Inc.
FDA (openFDA food enforcement)
Reported Dec 24, 2025
Hollandia Dairy, Inc. 100% Appleberry Juice; Half Pint (236mL). UPC: 0 27495 03679 6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hollandia Dairy, Inc.
FDA (openFDA food enforcement)
Reported Dec 24, 2025
HemosIL SynthAFax. Partial Thromboplastin Time Tests.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Instrumentation Laboratory
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed, resealable stand-up pouches in 8 oz, 1 lb., 2…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lexunder Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 24, 2025
Belevini KORUSHKA, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK, 20 PACKAGES PER CASE, FROZEN,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.MAMTAKIM, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 24, 2025
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
InPen App, Model/CFN Number: MMT-8061 (Android Users)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Hardware configuration of the BeneVision Central Monitoring System (CMS), marketed as BeneVision Distributed Monitoring…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Myosa for Kids KS1 REF MyOSAKS1_Sb/Sp/Mb/Mp/Lb/Lc KS2 REF MyOSAKS2_Sb/Sc/Mb/Mc/Mp/Lb/Lc Myosa for Kids is a mouthguard…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Myofunctional Research Company USA
FDA (openFDA device enforcement)
Reported Dec 24, 2025
2% Xylocaine DENTAL with Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novocol Pharmaceutical
6 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 24, 2025
MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe (P/N 8-69-41100)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Path
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Ondansetron ODT Tablets, USP 4mg, 1x10 unit dose tablets, Mfg: Glenmark Pharmaceuticals Limited, Repackaged by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preferred Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Dec 24, 2025
Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-12-PK…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rocket Medical PLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
FDA (openFDA device enforcement)
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