Pedialyte Unflavored (Export to Canada) 2 fl oz plastic reclosable bottle 48 count case
Abbott Laboratories
Compromised seal integrity which could lead to spoilage
95,018 total recalls in our database
Abbott Laboratories
Compromised seal integrity which could lead to spoilage
Abbott Laboratories
Compromised seal integrity which could lead to spoilage
Abbott Laboratories
Compromised seal integrity which could lead to spoilage
Par Formulations Private Limited
Failed Impurities/Degradation Specifications
ImprimisRx NJ
Subpotent Drug: The batches contain less than 90% of the labeled amount of latanoprost.
Nephron Sterile Compounding Center
CGMP Deviations: Potential for cross contamination due to product carry over.
Nephron Sterile Compounding Center
CGMP Deviations: Potential for cross contamination due to product carry over.
Lack of assurance of sterility: Bags have the potential to leak in the flexible containers which may compromise sterility.
CGMP Deviations: Other lots of hand sanitizer are being recalled because they were manufactured under the same conditions as the product lot found to contain methanol.
Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL BASED HAND SANITIZER isopropyl alcohol 75% v/v to contain methanol.
Failed Tablet/Capsule Specifications: Tablets exceeds specification for weight and thickness.
Failed Stability Specifications
Carefusion 2200
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Carefusion 2200
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
DeVilbiss Healthcare
An unapproved adhesive used to manufacture the accumulator tank sub assembly (a part of the patient gas pathway)
Product may not be sterile
The firm has become aware of PDM battery issues, including battery swelling, fluid leaking from the battery, and extreme overheating, which may pose a fire hazard. The firm has received a complaint alleging fire as a result of thermal energy from a DASH PDM.
Texas Medical Technology
Surgical gowns recalled due to gown fabric failing to pass the hydrostatic pressure test so the fabric does not provide the protection needed in a level 3 surgical gown, i.e., blood and other fluid may penetrate the fabric.
Carefusion 2200
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Getinge Usa Sales
The back rest may unintentionally drop suddenly, resulting in adverse health consequences if a patient were to fall on the floor head first and at a steep angle.