Recall archive
31,892 recalls · page 284 of 1329
Reported Jan 24, 2024
Lettuce in clear plastic 2lb bags.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorpated
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 24, 2024
Maquet PowerLEDII OR Light System, Model Names and Catalog Numbers PWDII77SF - ARDPWT629100A, PWDII555DF -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge USA Sales Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
ExcelsiusGPS Flat Panel Fluoroscopy Fixture Kit, Part number 6203.2100
High riskUsing this product could cause serious injury, illness or death — stop using it now.Globus Medical, Inc.
FDA (openFDA device enforcement)
Reported Jan 24, 2024
VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate, Item #454297, 13x75 grey cap-black ring, non-ridged.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greiner Bio-One North America, Inc.
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Haleon recalls Robitussin Cough syrups due to Microbial Contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Haleon
FDA (recalls & safety alerts)
Reported Jan 24, 2024
Herold's Salads -Potato Salad packaged in 1lb, 2lb, 5lb, and 10lb plastic tubs.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Herold Salads, Inc.
31 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 24, 2024
Ministry of Snacks Sweet and Savory Collection #8700
High riskUsing this product could cause serious injury, illness or death — stop using it now.Houdini Inc.
FDA (openFDA food enforcement)
Reported Jan 24, 2024
Americaine, (benzocaine 20%) Benzocaine Topical Anesthetic Spray, Aerosol Can 2 oz (57 G), Dist. by Insight…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company
FDA (openFDA drug enforcement)
Reported Jan 24, 2024
TECNIS Toric II OptiBlue IOL Models ZCW
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
FDA (openFDA device enforcement)
Reported Jan 24, 2024
PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.25MM…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Limacorporate S.p.A
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Product REF 4000-100N, DRAIN, EXPRESS SINGLE W/AC, Single Collection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maquet Cardiovascular, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Enfamil Nutramigen Hypoallergenic Infant Formula Powder with Iron cans (12.6 OZ and 19.8 OZ). UPC Code of 300871239418…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mead Johnson & Company LLC
FDA (openFDA food enforcement)
Reported Jan 24, 2024
Spanakopita, 6 oz (3 oz each piece), in plastic clam shell container
High riskUsing this product could cause serious injury, illness or death — stop using it now.NBRBDR Inc. dba Nutritious Delicious Foods
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 24, 2024
Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination table
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oakworks Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Soltive SuperPulsed Laser System TFL Fiber Stripper, Model Numbers TFL-AFS150, TFL-AFS200, TFL-AFS365, TFL-AFS550,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Vasostrict (vasopressin in 5% Dextrose) Injection, 20 units per 100 mL (0.2 units per mL), 100 mL x 10 Single Dose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Par Sterile Products LLC
FDA (openFDA drug enforcement)
Reported Jan 24, 2024
High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123
High riskUsing this product could cause serious injury, illness or death — stop using it now.Percussionaire Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pfizer Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Jan 24, 2024
Good Neighbor Pharmacy, DYE FREE, SUGAR FREE Magnesium Citrate Saline Laxative, Oral Solution, Cherry Flavor 10 fl. oz,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharma Nobis LLC
4 more products in this recall
FDA (openFDA drug enforcement)
Reported Jan 24, 2024
INDICAID COVID-19 Rapid Antigen At-Home Test, REF: P0040
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phase Scientific International Limited
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Incisive CT, Model Numbers 728144 and 728143. Computed Tomography X-Ray System PIM cable part number 459801179871
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
Calibration Serum Level 3. CAL 3, REF CAL2351. Human Assayed Multi-Sera Level 2 (HN1530) Human Assayed Multi-Sera Level…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 24, 2024
regard Operative LAP, Item Number 800943001; surgical convenience kit
High riskUsing this product could cause serious injury, illness or death — stop using it now.ROi CPS LLC
FDA (openFDA device enforcement)
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