95,114 total recalls in our database
AstraZeneca Pharmaceuticals
Presence of Foreign Tablets/Capsules: Confimed customer compliant by a retail pharmacist that an unopened bottle labeled as NEXIUM¿ capsules contained 60 SEROQUEL¿ XR tablets.
Failed Impurities/Degradation Specifications; 12 month stability testing (Expansion of RES #70548).
Superpotent Drug: Out Of Specification (OOS) result for Assay.
Subpotent drug
Failed Stability Specification: out of specification result obtained for the Particle Size Distribution test during stability testing.
CGMP Deviations: Failure of the manufacturer, Wockhardt Ltd, to adequately investigate customer complaints.
Dr. Reddy's Laboratories
Subpotent drug
Subpotent drug
Dr. Reddy's Laboratories
Failed Dissolution Specifications; exceeded specification at the 9 hour time point
Failed Dissolution Specifications; exceeded specification at the 9 hour time point
Failed Stability Specification: out of specification result obtained for the Particle Size Distribution test during stability testing.
Certain lots of the 3.7mm Cannulated Locking Screws and 3.7mm Cannulated Conical Screws were found to have been labeled incorrectly.
Complaints (including one reported death) allegedly of the lift arm drifting down suddenly. If the lift arm assembly is manually lifted, the actuator can become damaged and get stuck in the highest position. If a patient is lifted into the sling while the actuator is stuck, there is a potential risk of a free fall of the patient, resulting in minor or potentially catastrophic injuries.
Certain affected parts and lots of the Pull Reduction Devices may have been manufactured to an incorrect hardness specification which could result in intraoperative breakage.
Beaver-Visitec International
Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
Potential breach in sterility
Stryker initiated a device recall of the Navigation System II-Cart, Camera Articulated Arm because there is a potential that the weld seam between the main stud and the two flaps on the Articulated Arm was not welded in the correct location, which may result in a potential failure of the arm joint.
An issue with the cancel functionality used during atypical infusion programming to cancel user inputted values. An infusion may start that is greater than or less than the hospital established limits for the specific medication.
Intuitive Surgical
The coating of the 5 mm Thoracic Grasper main tube may experience damage with the possibility of fragments of coating material dislodging and potentially falling into patient.
Smiths Medical has become aware of an issue with an intermittent occurrence of binding of the locking assembly on some CADD¿-Solis pumps. Binding of the Cassette/ Keypad Lock can occur after latching the CADD¿-Solis Medication Cassette Reservoir or Administration Set disposable to the pump. When binding occurs, it can prevent the key from fully rotating the Cassette/ Keypad Lock to the locked (e