Recall archive
31,892 recalls · page 300 of 1329
Reported Nov 29, 2023
Model 97745 Controller used with Models 97715 and 97716 Intellis Neurostimulators
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Nov 29, 2023
DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Musculoskeletal Transplant Foundation, Inc.
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Buspirone Hydrochloride Tabs USP 10 mg, packaged in a) 15-count blister card (NDC 0615-7718-05) b) 30-count blister…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NCS Healthcare
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 29, 2023
Achieva 1.5T
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Tina-quant D-Dimer Test System, Fibrinogen/Fibrin Degradation Products Assay, Material Numbers 03001245322 - (cobas c…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Nov 29, 2023
stryker Sage PrimaFit External Urine Management System for the Female Anatomy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sage Products Inc.
FDA (openFDA device enforcement)
Reported Nov 29, 2023
IRON assay, Reference Numbers 6K95-41 and 6K95-30
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sentinel CH SpA
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SunMed Holdings, LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Polyvinyl Alcohol 1.4% Lubricating Eye Drops, packaged in 0.5 FL OZ (15mL) bottles, Dist. by: RUGBY LABORATORIES,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Nov 29, 2023
HEB Central Market Blueberry Buckwheat Gluten Free Waffle, 8.25oz, UPC 004122025365 Giant Eagle Blueberry Gluten Free…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Treehouse Foods
FDA (openFDA food enforcement)
Reported Nov 29, 2023
VariSoft infusion set, Model Number 1002827
High riskUsing this product could cause serious injury, illness or death — stop using it now.Unomedical A/S
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2023
Hilltop Meadow Farm recalls Hilltop Meadow Farm Pepper Jack Raw Milk Cheese due to Presence of Listeria monocytogenes
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Hilltop Meadow Farm
FDA (recalls & safety alerts)
Reported Nov 28, 2023
Kwik Trip, Inc. recalls Kwik Trip Fruit cups and trays containing cantaloupe. due to Potential to be contaminated with Salmonella.
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Kwik Trip, Inc.
FDA (recalls & safety alerts)
Reported Nov 22, 2023
Atrium Advanta V12 Covered Stent System, 10mm x 59mm x 80cm (OUS)-Indicated for restoring and improving the patency of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atrium Medical Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 22, 2023
AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical Division
FDA (openFDA device enforcement)
Reported Nov 22, 2023
CF Dallas, LLC recalls Seasonal Blend, Melon Trio and more Cantaloupes due to Potential Foodborne Illness, Salmonella
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.CF Dallas, LLC
FDA (recalls & safety alerts)
Reported Nov 22, 2023
ORALE! CAMARON MOLIDO, GROUND SHRIMP, NET WT. 2 OZ. 57 g (in paper cartons) (12 packages per case of 2 oz each), PACKED…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.EL Chilar-HF, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 22, 2023
Oxygen, Compressed USP, UN 1072, packaged in cylinders labeled as Size: a) C; b) D; c) E; d) H; e) M; f) M6, Rx only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Family Medical Supply Inc.
FDA (openFDA drug enforcement)
Reported Nov 22, 2023
Item 19858, Amazon Fresh, Frosted Mini Brownie with yellow and purple icing with sprinkles, 12 count per pack, packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Give and Go Prepared Foods Corp.
FDA (openFDA food enforcement)
Reported Nov 22, 2023
IBA Proton Therapy System - PROTEUS 235. PTS-11 versions, PTS-12 versions with Orion PPS version OSS6.0. Configured…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Consumer productsReported Nov 22, 2023
Lenovo Recalls USB-C Laptop Power Banks Due to Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lenovo Inc.
CPSC
Reported Nov 22, 2023
ADLT BLOOD CULTURE COLLECT KIT, REF DYNDH1245
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
4 more products in this recall
FDA (openFDA device enforcement)
Consumer productsReported Nov 22, 2023
MI Windows and Doors Recalls Vinyl Sliding Glass Doors Due to Serious Injury Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.MI Windows and Doors LLC
CPSC
Reported Nov 22, 2023
KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
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