Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for…
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for…
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for…
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for…
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for…
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results…
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
CGMP Deviations: cleaning procedures during manufacturing caused out of specification results for unknown impurities.
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
CGMP Deviations: Detection of trace amounts of NDMA, a possible impurity or contaminant in an active pharmaceutical ingredient.
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
Failed dissolution specifications: Out-of-Specification dissolution test result obtained during routine stability testing.
CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results…
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
Subpotent drug: During testing of the retention sample, the firm discovered that the product was sub-potent.
Lack of Assurance of Sterility: complaints received about dried powder on the outside of the bottle
Lack of assurance of sterility: loss of container integrity.
CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results…
Failed Impurities/Degradation Specifications:Out of specification result noticed for total impurities observed during stability analysis
Defective Container: Repetitive complaints received indicating pump not working.
Kia Motors America (Kia) is recalling certain 2019 Kia Forte vehicles equipped with LED headlights. The headlights may not have been manufactured with the correct low beam aiming. As such,…
Browse recent months with enough recall history for useful comparison.
