95,114 total recalls in our database
Whole Foods Market
The product has the potential to be contaminated with Listeria monocytogenes.
Cheesecake Royale
Recalled product contains undeclared walnuts. Walnut is not listed on the ingredients statement, however pecans are listed as an ingredient.
Whole Foods Market
The product has the potential to be contaminated with Listeria monocytogenes.
Whole Foods Market
The product has the potential to be contaminated with Listeria monocytogenes.
Fresenius Kabi USA
Lack of Assurance of Sterility: Glass vials may have finish fractures and glass particles.
Sandoz Incorporated
Labeling: Illegible Label: Sandoz Inc. is recalling of one lot of Fluoxetine Capsules due to an illegible logo on the capsule.
Fresenius Kabi USA
Defective Container: Vials may be missing stoppers.
Fresenius Kabi USA
Lack of Assurance of Sterility: Glass vials may have finish fractures and glass particles.
CareFusion 213
Does Not Meet Monograph: Chlorhexidine Gluconate Surgical Scrub Brush is being recalled due to higher concentrations of available chlorhexidine gluconate.
Presence of Particulate Matter: Baxter Healthcare Corporation has received a complaint reporting the presence of particulate matter identified as plastic/rubber in famotidine Injection premixed containers.
Fresenius Kabi USA
Lack of Assurance of Sterility: Glass vials may have finish fractures and glass particles.
Lack of Assurance of Sterility; improperly crimped fliptop vials
Failed Tablet/Capsule Specifications: Product being recalled due to the potential presence of cracked or broken capsules.
Tubing may detach at the connect/disconnect location on the MiniMed Silhouette and MiniMed Sure-T infusion sets. Detachment causes interrupted insulin delivery and the pump will not alarm to notify your patient. This can lead to hyperglycemia, and diabetic ketoacidosis (DKA).
Siemens Medical Solutions USA
Printouts may be printed in incorrect anatomical size when using syngo.plaza or syngo Imaging XS filming application in conjunction with a printer not released for anatomical print usage. This may happen due to an invalid combination of printer and the syngo.plaza printer configuration file. Printouts in anatomical size are not correct and may influence diagnostic decisions and/or therapy.
Biomet Microfixation
Laser etching on the parts is wider and deeper than the conditions previously validated.
In certain operating room environments, a colored screen image occurs with the 1488 Cameras that were manufactured during a specific time period
Instrumed International
The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet all FDA requirements to market the devices as "Pre-Amendment" devices.
The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet all FDA requirements to market the devices as "Pre-Amendment" devices.
Instrumed International
The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet all FDA requirements to market the devices as "Pre-Amendment" devices.