Complete FDA and NHTSA recall records dated in April 2019.
These records include useful source details for the selected month.
Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Presence of Particulate Matter.
Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Presence of Particulate Matter.
Presence of Particulate Matter.
Lack of Assurance of Sterility: Product is not terminally sterialized and not tested per USP 71.
Defective container: Ineffective seal between the cap and jar of the affected product.
Subpotent Product: assay results for Amoxicillin were below the specification limits.
Failed Impurities/Degradation Specifications: Unknown impurity above specification limits.
Lack of Assurance of Sterility: environmental monitoring report exceeds limits, therefore sterility cannot be assured.
cGMP deviations: Product was exposed above 50% relative humidity levels during packaging operations.
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be tainted with undeclared sildenafil and tadalafil, two FDA approved drugs for the treatment of male erectile…
Nissan North America, Inc. (Nissan) is recalling certain 2019 Altima vehicles equipped with front wheel drive (FWD) and 2.5 liter engines. The fuel pump lock ring may not be fully engaged,…
The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.
There is a potential risk of a wrong measurement in the annulus plane during a TAVI planning procedure. This risk is due to a software issue found in the TAVI algorithm.
Complaints regarding loose proximal body bolts or bolts that were found through x-ray as sitting above the proximal body and not properly seated. Patient risks may include: pain,…
There is a potential risk of a wrong measurement in the annulus plane during a TAVI planning procedure. This risk is due to a software issue found in the TAVI algorithm.
The product lidstock contains a labelling error. The lidstock states the incorrect priming volume. The priming volumes printed on the extension lines are correct
Edwards Lifesciences has received a limited number of customer reports regarding an inter-lumen leak between the cardioplegia lumen and pressure lumen in the device.
Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double Bevel knife however, the marking on device shows a 2.75mm size device
There is a potential to generate incorrect results on the instrument if particular error codes are not resolved before transitioning to the Running status.
There is the potential for debris/material to be found behind the O-rings in the neck trials.
During manufacturing of an Azurion R2.0 system, it was found out that the cable set was not according to specification. This resulted in damage of the 24V power cable of the detector.
Temperature indicator may have changed color to dark gray or black prior to shipment. Change in color may indicate the product exposure to temperatures greater than 110¿F
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
