95,018 total recalls in our database
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Dr. Berne's Whole Health Products
Non-Sterility
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Central Admixture Pharmacy Services
Lack of assurance of sterility:
Subpotent: Failing Test Results for Epinephrine
GE MEDICAL SYSTEMS, ISRAEL
Some Venue Go Standard Carts can develop an internal failure of the vertical/horizontal tilt adjustment mechanism which can result in the Venue Go system detaching from the cart and falling.
Boston Scientific
Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were distributed with a tip curve shape which differs from the labeled tip curve shape.
Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic Navigation System, SPiN Planning Laptop Workstation, and all associated navigation instruments) manufacturing to design requirements and insufficient evidence to demonstrate adequate electromagnetic compatibility (EMC). EMC is the ability of electrical equipment and systems to function acceptably without interference and to not interfere with other devices within its operating environment
Boston Scientific
Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were distributed with a tip curve shape which differs from the labeled tip curve shape.
19-gauge x 1" inch filter needles showed appearances of a small fraction of non-preferred characteristics. A causal relationship has not been established between the structural variations in this 19-gauge filter needle and the rare events of retinal vasculitis
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.