Recall archive
31,892 recalls · page 95 of 1329
Reported Dec 3, 2025
Brand Name: Single Use Ligating Device Product Name: Olympus HX-400U-30 Model/Catalog Number: HX-400U-30 Used with an…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olympus Corporation of the Americas
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Philips Azurion 7M20 systems with FlexArm ceiling-mounted system. Model Number: 722234;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Quantum Intersegmental Table, Model/Catalog Number: Q400; heated massage table
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pivotal Health Solutions, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2025
1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel, Inc.
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Emdogain; Article Numbers: (1) 440.230V10, (2) 475.132V10;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
FDA (openFDA device enforcement)
Reported Dec 3, 2025
NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Whatcom Blue Sliced cheese; Sliced and packaged in deli plastic wrap with Whole Foods Scale labels.
High riskUsing this product could cause serious injury, illness or death — stop using it now.WFM Purchasing, LP
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 2, 2025Updated Aug 26, 2026
Mondelez Global LLC recalls Ritz Peanut Butter Cracker Sandwiches due to Potential or Undeclared Allergen – Undeclared Peanut
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Mondelez Global LLC
FDA (recalls & safety alerts)
Reported Dec 2, 2025Updated Aug 26, 2026
Vetoquinol USA recalls Vetoquinol FOLLTROPIN Injectable Kits for Cattle due to Presence of particulate matter
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Vetoquinol USA
FDA (recalls & safety alerts)
Reported Nov 26, 2025
Fesoterodine Fumarate, Extended-release Tablets, 4 mg, 30-count bottle, Rx only, Manufactured by: Alembic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alembic Pharmaceuticals Limited
FDA (openFDA drug enforcement)
Reported Nov 26, 2025Updated Aug 26, 2026
Anthony’s BBQ Sauce recalls Anthony’s Barbecue Sauce due to May contain undeclared Anchovy (fish).
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Anthony’s BBQ Sauce
FDA (recalls & safety alerts)
Reported Nov 26, 2025
SAFE-T-FILL Micro Capillary Blood Collection, 125 ¿L; Prepared with Lithium Heparin; Green Model/Catalog Number: 07…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ASP Global, LLC. dba Anatomy Supply Partners, LLC.
23 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2025
MONARCH Bronchoscope. Model Number: MBR-000211-B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health, Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
DxFLEX Flow Cytometer Catalog Number C78500 UDI-DI code: 15099590754013 The DxFLEX Flow Cytometer is intended for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Nov 26, 2025
Tribio Implant 7.5mm x 40mm REF M80 SB008 UDI code: (01) 00816125023653(10) EBL10B13C(17) 270630 Tribio" Implant is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Berkeley Advanced Biomaterials, LLC
FDA (openFDA device enforcement)
Reported Nov 26, 2025
Bulk and Organic Organic Moringa Powder, 44.1lbs bag
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bulk & Organic LLC
FDA (openFDA food enforcement)
Reported Nov 26, 2025
BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY ONE PIECE BEZEL 8100,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cellavision AB
FDA (openFDA device enforcement)
Consumer productsReported Nov 26, 2025
Ozark Trail Tabletop 1-Burner Butane Camping Stoves Recalled Due to Serious Burn and Fire Hazards; Imported and Sold by…
High riskUsing this product could cause serious injury, illness or death — stop using it now.China Window Industry Co., Ltd.
CPSC
Reported Nov 26, 2025
4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%, 113g, (4 oz) per bottle, DermaRite Industries LLC, 7777…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DermaRite Industries, LLC
17 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 26, 2025
MOSAIQ Oncology Information System Software Builds 3.1.3, 3.2.1, 3.2.2 & 3.2.3.0 Software Version and UDI Codes:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta Solutions Ab
FDA (openFDA device enforcement)
Reported Nov 26, 2025
Brand Name: Equinoxe Ergo Product Name: Adjustable Angle rTSA Reamer, 42mm Model/Catalog Number: 321-59-42 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 26, 2025
NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: Kremers Urban…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Medical Supply Inc.
FDA (openFDA drug enforcement)
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