Venlafaxine Hydrochloride Extended-Release Capsules, USP 37.5mg recall — FDA D-0617-2024
Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
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.
Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were incorrectly labeled as Ferrum Metallicum 200C.
Hyundai Motor America (Hyundai) is recalling certain 2024 Santa Fe and Santa Fe HEV vehicles. The main floor wiring harness may chafe against the passenger-side second-row bench seat…
Failed Dissolution Specifications: results below specifications
This product is being recalled due to the tube weld failure presents itself as a slow leak and can be difficult to detect.
CGMP Deviations
Failed Impurities/Degradation Specifications: Product is being recalled due to API related substances and unknown impurities that are above the specification limits.
Failed Dissolution Specifications
Failed Dissolution Specifications
Microbial Contamination of Non-Sterile Products: confirmed presence of mold contamination
Failed Dissolution Specifications
Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism
CGMP Deviations
Tesla, Inc. (Tesla) is recalling certain 2021-2024 Model 3, Model S, Model X, and 2020-2024 Model Y vehicles. The hood latch assembly may fail to detect an unlatched hood condition after…
Gulf States Toyota, Inc. (GST) is recalling certain Toyota 2023 GR Supra, 2024 4 Runner, Corolla, Grand Highlander, Grand Highlander Hybrid, Land Cruiser Hybrid, Tacoma, Tacoma Hybrid,…
Subpotent Drug: reduced efficacy for epinephrine
Cross contamination with other products
Lack of Assurance of Sterility: Potential presence of leaks originating from the Connector Assembly component.
CGMP Deviations: Manufactured without following Current Good Manufacturing Practises.
Failed Impurities/Degradation Specifications: The impurity results at 12 months stability testing,did not conform to the specification limit.
Microbial Contamination of Non-Sterile Products: Presence of Aspergillus Sydowii (Mold)
CGMP Deviations
Failed Dissolution Specifications; the product is dissolving faster than the specified limits.
Cross contamination with other products
Browse recent months with enough recall history for useful comparison.