Medline Industries recalls 2,980 medical convenience kits containing NAMIC angiographic rotating adapter syringes due to risk of adapter unwinding causing disconnection during use; distributed nationwide in US, Puerto Rico, Canada, Netherlands, and …
FDA Class I recall of Blue Bull Extreme Male Enhancement Supplement by Pure Vitamins and Natural Supplements, LLC for undeclared sildenafil; distributed in New Jersey.
Fagron Compounding Services recalls 16,130 bags of vancomycin HCI and four other sterile products nationwide due to failed sterility assurance and potential port detachment risks.
Cipla USA recalls Lanreotide Injection 120 mg/0.5 mL nationwide due to sterility assurance deficiencies at the contract manufacturer's visual inspection procedure.
Cook Medical recalls 20 units of Arterial Pressure Monitoring Trays (APMY series) distributed worldwide due to expiration date labeling exceeding true shelf life, posing temporary health risks.
FDA seeks public comments on financial transparency and efficiency of prescription drug, biosimilar, and generic drug user fee programs at a public meeting.
Stryker Sustainability Solutions recalls 56,740 tourniquet cuffs nationwide due to potential detachment at welding connections that could compromise pressure maintenance.
FDA holds public meeting on expanding nonprescription drug access and requests stakeholder comments; no specific deadline or financial impact stated for small businesses.
Molded Products Inc. voluntarily recalls 26,900 units of MPC-130 See Luer Cap Set nationwide due to threaded sleeve detachment risk, classified as Class II medical device recall.
Beckman Coulter recalls 3 boxes of MicroScan Neg Multidrug Resistant MIC test panels distributed to Poland due to manufacturing defects that may cause incorrect in vitro diagnostic results.
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