Philips, HeartStart HS1 Home Defibrillator, Model # Model number: M5068A
Philips North America
Customers were not notified of previous recalls associated with various defibrillator models.
95,114 total recalls in our database
Philips North America
Customers were not notified of previous recalls associated with various defibrillator models.
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Sandwiches may contain undeclared soy and egg.
The Earl of Sandwiches
Sandwiches may contain undeclared soy and egg.
Sandwiches may contain undeclared egg.
Vintage Food
Undeclared sulfites
The Earl of Sandwiches
Sandwiches may contain undeclared soy and egg.
The firm was notified by one of their customers that during a random testing by ODA the product test positive for Listeria monocytogenes.
The Earl of Sandwiches
Sandwiches may contain undeclared soy and egg.
It was discovered that bottles of Brain and Memory Power Boost was filled with multi vitamin-mineral product - NeuroVite Plus
Marketed Without an Approved NDA/ANDA: FDA analysis determined the presence of tadalafil
Product Mix-up: Incorrect diluent component included in the kit.
Microbial Contamination of Sterile Products: Confirmed sterility failure identified during stability testing at the 12-month time point.
Lack of Assurance of Sterility: Air filter failed post integrity test leading to a lack of sterility assurance.
Labeling: Incorrect Instructions
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Some devices are outside tolerances and showed a maximal deviation of 2 degrees in the orientation between the peek head and titanium base, and an incongruence between the size engraved on the peek has been identified. Deviations may delay the final restoration.
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials will cause the instrument to generate a warning that calibrators are incorrectly loaded and calibration will not be completed successfully.
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing