Recall archive
31,892 recalls · page 277 of 1329
Reported Feb 14, 2024
Sperm separation media are used to separate motile sperm from other constituents of semen.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujifilm Irvine Scientific, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
FLEXSelect 5/16" Amber Latex Elastics-Intended use is orthodontics, braces, tooth gap, Ref: AMD56
Moderate riskThis product could cause temporary or reversible health problems — stop using it.G & H Wire Company
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Senographe Pristina
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, SCS
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Flow-i C20 Anesthesia System, model 6677200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Globus Medical Cranial Drill with Stop, 2.40mm - Instruments for access, preparation, and placement of cranial devices…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Globus Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
RESER'S POTATOE POTATOES MASHED RED SKN 4/5# SUPC/ITEM # 3264
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greco Sidari
35 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 14, 2024
HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use, sterile surgical instruments used during hip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Article No. NA6050411, Valiant PhD No. 1 Econo
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ivoclar Vivadent, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
CVS Health brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%), packaged in a) 0.5 FL OZ (15mL) bottles…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kilitch Healthcare India Limited
21 more products in this recall
FDA (openFDA drug enforcement)
Reported Feb 14, 2024
BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating, Product Code 701047554. For use with an extracorporeal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Medline Remedy Clinical TREAT Antifungal Cream, 2% Miconazole Nitrate, Paraben Free, 4 FL OZ (118 mL) tube,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
FDA (openFDA drug enforcement)
Reported Feb 14, 2024
Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Authentic Fresh to You Deluxe Triple Decker Club Net Wt. 8.8oz (254g). Product packaged in a plastic PET container.
High riskUsing this product could cause serious injury, illness or death — stop using it now.MG Foods Middletown
FDA (openFDA food enforcement)
Reported Feb 14, 2024
Ito-Shoten Seasoned Mushroom 200g/7.06 oz. Product of Japan Distributed by Mitsuwa Corporation Torrance, CA 90501
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mitsuwa Corporation
FDA (openFDA food enforcement)
Reported Feb 14, 2024
Lansoprazole Delayed-Release Capsules USP, 15 mg, 14-count bottle, Manufactured by: Natco Pharma Limited Kothur- 509…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NATCO Pharma Limited
FDA (openFDA drug enforcement)
Reported Feb 14, 2024
Protocol for Life Balance, Phosphatidyl Serine 300mg softgels, 50 count bottle, UPC 707359123922. NOW Foods,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Now Foods
FDA (openFDA food enforcement)
Reported Feb 14, 2024
Olympus/Gyrus Paparrela-Type Vent Tube 1.02MM, Silicone, Sterile- to ventilate the middle ear subsequent to otitis…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Omeza Lidocaine Lavage pain relief oil 10*2mL VIALS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Omeza LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Feb 14, 2024
Spectral CT on Rails: Software Version 5.1.0.X, model 728334.
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 14, 2024
BrightView, gamma camera system; Model Nos.: 6-digit format 882480; 12-digit format 453560279781 453560279791…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips North America
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
RX Series Copper (Cu) Assay Ref. Number CU2340
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
1. HeartMate Touch Communication System, REF HMT1100 2. HeartMate Touch Communication System, Rental REF HMT1100-R 3.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Thoratec Corp.
FDA (openFDA device enforcement)
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