Complete FDA and NHTSA recall records dated in 2023, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Elekta has identified that if the microswitch within the middle arm is incorrectly setup, there is a potential for an uncontrolled extension of iViewGT / XVI detector arms. When the…
Elekta has identified that if the microswitch within the middle arm is incorrectly setup, there is a potential for an uncontrolled extension of iViewGT / XVI detector arms. When the…
Defect in the outer packaging of the Cranial Access Kits. can cause the packaging to split without any additional forces outside compromising the sterility of the device
Their is a potential that intraocular implant devices may not meet specifications.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5, Green 3.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6.
During an FDA inspection the firm was notified that some of their products contains undeclared soy and Yellow #5 & #6.
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5 & #6 and Blue 1.
The affected product is being recalled from the marketplace due to possible Salmonella contamination.
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
During an FDA inspection the firm was notified that some of their products contains undeclared soy, Yellow #5 & #6.
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
salmonella
During an FDA inspection the firm was notified that some of their products contains undeclared soy and Yellow #6.
During an FDA inspection the firm was notified that some of their products contains undeclared soy.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5.
The affected product is being recalled from the marketplace due to possible Salmonella contamination.
Potential Salmonella contamination.
Product contains elevated levels of patulin
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5, Red 40 & 3 and Green 3.
During an FDA inspection the firm was notified that some of their products contains undeclared Yellow #5.
Potential Salmonella contamination.
salmonella
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.
