95,018 total recalls in our database
Renaissance Food Group
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Renaissance Food Group
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Renaissance Food Group
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Renaissance Food Group
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Renaissance Food Group
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Renaissance Food Group
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Renaissance Food Group
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Presence of Particulate Matter: Piece of metal found in a vial
Salon Technologies International
Chemical Contamination: product found to contain benzene
Lack of Assurance of Sterility: environmental monitoring failure.
Salon Technologies International
GMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Dr. Reddy's Laboratories
Failed Stability Specifications: Out of specification results reported at 12-month stability testing for aluminum content.
Woodbine Products Co
Labeling: Not Elsewhere Classified - Incorrect label-incorrect scent listed on label.
Presence of Particulate Matter: A complaint was received for the presence of a hair in one vial.
The outer sterile package cavity has a corner wall thickness that is below the specification. The thin corner wall could potentially crack during transit. Potential risks include non-clinically or clinically significant extension of surgery, or infection leading to surgical intervention.
Fresenius Kabi USA
The display screen may become frozen and unresponsive to user input, triggering an alarm that is evidenced by a buzzer sound and flashing red LEDs as a secondary notification. However, as the screen goes blank it does not indicate an alarm condition or respond. This issue leads to temporary cessation of flow of a medication or fluid, requiring immediate intervention by the clinician.
B Braun Medical
Potential for leakage at the catheter hub.
Philips Respironics
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Philips Respironics
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Philips Respironics
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.