Skip to main content

Pharmacy Learning Network

PharmLaw

FDA Recalls

In the News

News
09/10/2026
Rebecca Amrick
Trokendi (topiramate) extended-release capsules are under a voluntary Class III recall due to failed dissolution specifications, affecting 11 304 bottles.
Trokendi (topiramate) extended-release capsules are under a voluntary Class III recall due to failed dissolution specifications, affecting 11 304 bottles.
Trokendi (topiramate)...
09/10/2026
Pharmacy Learning Network
News
09/10/2026
Rebecca Amrick
A voluntary Class II recall has been issued for trazodone hydrochloride tablets after the firm discovered foreign tablets in the product, a discrepancy that affects 175 392 bottles.
A voluntary Class II recall has been issued for trazodone hydrochloride tablets after the firm discovered foreign tablets in the product, a discrepancy that affects 175 392 bottles.
A voluntary Class II recall has...
09/10/2026
Pharmacy Learning Network
News
09/10/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for famotidine injection due to Current Good Manufacturing Practice (CGMP) deviations.
The US Food and Drug Administration (FDA) has issued a Class II recall for famotidine injection due to Current Good Manufacturing Practice (CGMP) deviations.
The US Food and Drug...
09/10/2026
Pharmacy Learning Network
PharmLaw
09/09/2026
Hannah Musick
Florida has sued Express Scripts and Prime Therapeutics over allegations that the pharmacy benefit managers (PBMs) unlawfully coordinated pharmacy reimbursement rates, raising new antitrust and compliance questions surrounding PBM contracting...
Florida has sued Express Scripts and Prime Therapeutics over allegations that the pharmacy benefit managers (PBMs) unlawfully coordinated pharmacy reimbursement rates, raising new antitrust and compliance questions surrounding PBM contracting...
Florida has sued Express Scripts...
09/09/2026
Pharmacy Learning Network
News
09/03/2026
Rebecca Amrick
Acthar Gel (repository corticotropin) injection is under a voluntary Class II recall due to the presence of particulate matter, affecting 12 367 vials.
Acthar Gel (repository corticotropin) injection is under a voluntary Class II recall due to the presence of particulate matter, affecting 12 367 vials.
Acthar Gel (repository...
09/03/2026
Pharmacy Learning Network