95,075 total recalls in our database
Wells Enterprises
Foreign material (plastic) may be present in ice cream product
Wells Enterprises
Foreign material (plastic) may be present in ice cream product
May Flower International
Product contains undeclared wheat.
Wells Enterprises
Foreign material (plastic) may be present in ice cream product
Wells Enterprises
Foreign material (plastic) may be present in ice cream product
Wells Enterprises
Foreign material (plastic) may be present in ice cream product
Product contains undeclared sulfites (7.49mg/serving)
Undeclared allergens (milk and/or peanuts).
Wells Enterprises
Foreign material (plastic) may be present in ice cream product
Undeclared Almonds
cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm voluntarily recalled all La Roche-Posay Effaclar Duo Dual Action Acne Treatment lots.
Chemical Contamination: This recall has been initiated due to detected trace levels of benzene.
Lack of Assurance of Sterility
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.
Balloon extension lumens are not printed correctly. Specifically, the inner balloon inflation hub was labeled as the outer balloon, and the outer balloon inflation hub was labeled as the inner balloon.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.
MEDLINE INDUSTRIES, LP - Northfield
Three is the potential for the retractors to puncture through the sterile packaging.
Beckman Coulter is recalling their DxC 500 AU Clinical Chemistry Analyzer because a software error causes the analyzer to not run a requested calibration order in the following scenario: when a reagent blank or calibration is ordered during sample processing and then any of the components (R1 and/or R2) depletes to zero tests, the analyzer will not be able to complete the calibration request, and the calibration order will remain pending. No further calibration orders can be processed for any assays, and the instrument refuses to accept further sample processing order after the existing calibration curves are expired. Although in-process tests will be completed, this error can cause a delay in reporting subsequent test results. No further calibration orders can be processed for any assays which may cause a delay in reporting test results.