Overview of recall records associated with Sun Pharmaceutical Industries, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 80, Class III: 32, Class I: 3.
Presence of Foreign Substance:Sun Pharma is recalling one (1) lot of Sulfamethoxazole and Trimethoprim Tablets USP, 800 mg/160 mg (500 ct.) because a foreign matter identified as…
Sun Pharmaceutical is recalling Azelastine HCl Nasal Solution, 0.1% (30 mL Bottle) following a failure to meet the % RSD requirement in the test for Droplet Size during the 6 month long…
Lack Of Assurance Of Sterility
Microbial Contamination of Non-Sterile Products
Failed Tablet/Capsule Specifications: out of specification results for increased tablet hardness.
Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Presence of Foreign Substance: consumer complaint for foreign matter embedded in the tablet identified as a broken piece of wire rope from the manufacturing equipment.
Failed Dissolution Specifications
Failed Dissolution Specifications; 18 month stability time point
Failed Dissolution Specifications; 18 month stability time point
Failed Stability Specifications: Low Out of Specification results for alcohol content.
Failed Dissolution Specifications
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
Failed Impurities/Degradation Specifications
Crystallization; crystallized nimodipine
This page summarizes recall records in which the official source identifies Sun Pharmaceutical Industries, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
