Recall archive
31,892 recalls · page 275 of 1329
Reported Feb 21, 2024
Model No. BEQ-HLS 5050 USA, HLS Set Advanced 5.0, Product Code/Part Number 70106.9077. Used with the CARDIOHELP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Captus 4000e Thyroid Uptake Systems- Intended to be used by trained Nuclear Medicine Technologists or Nuclear Medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mirion Technologies (Capintec), Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Musculoskeletal Transplant Foundation, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuroLogica Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Single Use Distal Cover MAJ-2315 Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Accessory Sets Syringes: 6ml syringe with a female luer with 15cm sealed SCD tubing, REF: RF-T15, and 60ml syringe on a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OriGen Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
CombiDiagnost R90 1.0 (709030)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)706100 (2)706110
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a sandwich design that is used with Sofia 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Rico Brand recalls Rico Enchiladas due to Potential for Listeria monocytogenes contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Rico Brand
FDA (recalls & safety alerts)
Reported Feb 21, 2024
MobileDiagnost wDR, Model numbers 712001, 712002, 712004, 712006, and 712007
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal Sa
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons, each carton contains 3 blister…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Feb 21, 2024
HydrALAZINE Hydrochloride Tablets, USP 10mg, packaged in 100-count (10x10 blister cards), Lot T04680, Rx only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
FDA (openFDA drug enforcement)
Reported Feb 21, 2024
Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557357156, 721557357163 Dragonfly Jelly Bar Backpack 7.93oz,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.U.S. Tov, Inc.
FDA (openFDA food enforcement)
Reported Feb 21, 2024
Woodstock 5 Grain Cereal. Oats, Rye, Triticale, Barley, Golden Flax. Net Wt. 18.5 oz (1 lb 2.5 oz) 524g. UPC 0…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.UNFI General Corporate
FDA (openFDA food enforcement)
Reported Feb 21, 2024
Utz Wavy Originals Potato Chips, Net WT. 2.75 oz (78g), UPC 0-41780-19014-7.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Foods, LLC
FDA (openFDA food enforcement)
Reported Feb 21, 2024
GE Healthcare neonatal incubator, models: a) Care Plus, b) Care Plus 1000, c) Care Plus 2000, d) Care Plus 3000, e)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wipro GE Healthcare Private Ltd.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2024
Nordic Naturals recalls Nordic Naturals Baby’s Vitamin D3 Liquid due to Elevated level of Vitamin D3 dosage
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Nordic Naturals
FDA (recalls & safety alerts)
Reported Feb 17, 2024
Raw Farm LLC recalls Raw Farm LLC Raw Cheddar Cheese due to Potential contamination with E. Coli 0157:H7
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Raw Farm LLC
FDA (recalls & safety alerts)
Reported Feb 16, 2024
TRUONG GIANG DISTRIBUTOR CORP recalls Golden Owl Dried mango due to Undeclared sulfites.
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Truong Giang Distributor Corp.
FDA (recalls & safety alerts)
Consumer productsReported Feb 15, 2024
Bell Sports Recalls Bell Soquel Youth Bicycle Helmets Due to Risk of Head Injury; Violation of the Federal Safety…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bell Sports Inc.
CPSC
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