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FTC Settlement With Caremark Signals New Compliance Expectations for PBMs
07/15/2026
Hannah Musick
The Federal Trade Commission's (FTC) proposed settlement with CVS Caremark would require significant changes to pharmacy benefit manager (PBM) rebate practices, transparency, formulary management, and pharmacy contracting, signaling evolving...
The Federal Trade Commission's (FTC) proposed settlement with CVS Caremark would require significant changes to pharmacy benefit manager (PBM) rebate practices, transparency, formulary management, and pharmacy contracting, signaling evolving...
The Federal Trade Commission's...
07/15/2026
Pharmacy Learning Network
PharmLaw
Former Done Global CEO, Clinical President Sentenced in Telehealth Adderall Fraud Case
07/08/2026
Grace Taylor, MS, MA
Former executives of Done Global were sentenced to federal prison after convictions in a multimillion-dollar scheme involving unlawful telehealth prescribing of Adderall and health care fraud, according to the US Department of Justice.
Former executives of Done Global were sentenced to federal prison after convictions in a multimillion-dollar scheme involving unlawful telehealth prescribing of Adderall and health care fraud, according to the US Department of Justice.
Former executives of Done Global...
07/08/2026
Pharmacy Learning Network
PharmLaw
DOJ Telemedicine Fraud Case Underscores Compliance Risks for Health Care Organizations
07/01/2026
Hannah Musick
A US Department of Justice (DOJ) enforcement action against a telemedicine company owner underscores continuing regulatory scrutiny of telemedicine prescribing, kickback arrangements, and Medicare billing practices.
A US Department of Justice (DOJ) enforcement action against a telemedicine company owner underscores continuing regulatory scrutiny of telemedicine prescribing, kickback arrangements, and Medicare billing practices.
A US Department of Justice (DOJ)...
07/01/2026
Pharmacy Learning Network
PharmLaw
PBM Trade Group Challenges Illinois Drug Pricing Transparency Law on ERISA Grounds
06/24/2026
Hannah Musick
The Pharmaceutical Care Management Association has sued Illinois to block key provisions of the state's Prescription Drug Affordability Act, setting up a legal challenge that could shape the future of pharmacy benefit manager (PBM)...
The Pharmaceutical Care Management Association has sued Illinois to block key provisions of the state's Prescription Drug Affordability Act, setting up a legal challenge that could shape the future of pharmacy benefit manager (PBM)...
The Pharmaceutical Care...
06/24/2026
Pharmacy Learning Network
PharmLaw
Ahold Delhaize USA to Pay $40 Million in Drug Price Claims Settlement
06/16/2026
Grace Taylor, MS, MA
Ahold Delhaize USA agreed to pay $40 million to resolve allegations that supermarket pharmacies reported inflated usual and customary drug prices to federal health care programs.
Ahold Delhaize USA agreed to pay $40 million to resolve allegations that supermarket pharmacies reported inflated usual and customary drug prices to federal health care programs.
Ahold Delhaize USA agreed to pay...
06/16/2026
Pharmacy Learning Network

FDA Recalls

News
Clomiphene Citrate Recalled Due to CGMP Deviations
07/16/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for clomiphene citrate due to Current Good Manufacturing Practice (CGMP) deviations.
The US Food and Drug Administration (FDA) has issued a Class II recall for clomiphene citrate due to Current Good Manufacturing Practice (CGMP) deviations.
The US Food and Drug...
07/16/2026
Pharmacy Learning Network
News
Bortezomib Injections Recalled Due to Lack of Sterility Assurance
07/16/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for bortezomib injections due to a lack of sterility assurance, affecting 11 400 vials.
The US Food and Drug Administration (FDA) has issued a Class II recall for bortezomib injections due to a lack of sterility assurance, affecting 11 400 vials.
The US Food and Drug...
07/16/2026
Pharmacy Learning Network
News
Methohexital Sodium Injections Recalled Due to Failed Impurities/Degradation Specifications
07/16/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for methohexital sodium injections due to the product’s failure to meet impurities/degradation specifications, affecting 4284 vials.
The US Food and Drug Administration (FDA) has issued a Class II recall for methohexital sodium injections due to the product’s failure to meet impurities/degradation specifications, affecting 4284 vials.
The US Food and Drug...
07/16/2026
Pharmacy Learning Network
News
ADHD Medication Recalled Due to Incorrect Labeling
07/09/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for combination extended-release capsules of dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate due to a...
The US Food and Drug Administration (FDA) has issued a Class II recall for combination extended-release capsules of dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate due to a...
The US Food and Drug...
07/09/2026
Pharmacy Learning Network
News
Synjardy XR Tablets Recalled Due to CGMP Deviations
07/09/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for Synjardy XR (empagliflozin and metformin hydrochloride) tablets due to Current Good Manufacturing Practice (CGMP) deviations, affecting 560 bottles.
The US Food and Drug Administration (FDA) has issued a Class II recall for Synjardy XR (empagliflozin and metformin hydrochloride) tablets due to Current Good Manufacturing Practice (CGMP) deviations, affecting 560 bottles.
The US Food and Drug...
07/09/2026
Pharmacy Learning Network

In the News

News
Clomiphene Citrate Recalled Due to CGMP Deviations
07/16/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for clomiphene citrate due to Current Good Manufacturing Practice (CGMP) deviations.
The US Food and Drug Administration (FDA) has issued a Class II recall for clomiphene citrate due to Current Good Manufacturing Practice (CGMP) deviations.
The US Food and Drug...
07/16/2026
Pharmacy Learning Network
News
Bortezomib Injections Recalled Due to Lack of Sterility Assurance
07/16/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for bortezomib injections due to a lack of sterility assurance, affecting 11 400 vials.
The US Food and Drug Administration (FDA) has issued a Class II recall for bortezomib injections due to a lack of sterility assurance, affecting 11 400 vials.
The US Food and Drug...
07/16/2026
Pharmacy Learning Network
News
Methohexital Sodium Injections Recalled Due to Failed Impurities/Degradation Specifications
07/16/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for methohexital sodium injections due to the product’s failure to meet impurities/degradation specifications, affecting 4284 vials.
The US Food and Drug Administration (FDA) has issued a Class II recall for methohexital sodium injections due to the product’s failure to meet impurities/degradation specifications, affecting 4284 vials.
The US Food and Drug...
07/16/2026
Pharmacy Learning Network
PharmLaw
FTC Settlement With Caremark Signals New Compliance Expectations for PBMs
07/15/2026
Hannah Musick
The Federal Trade Commission's (FTC) proposed settlement with CVS Caremark would require significant changes to pharmacy benefit manager (PBM) rebate practices, transparency, formulary management, and pharmacy contracting, signaling evolving...
The Federal Trade Commission's (FTC) proposed settlement with CVS Caremark would require significant changes to pharmacy benefit manager (PBM) rebate practices, transparency, formulary management, and pharmacy contracting, signaling evolving...
The Federal Trade Commission's...
07/15/2026
Pharmacy Learning Network
News
ADHD Medication Recalled Due to Incorrect Labeling
07/09/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for combination extended-release capsules of dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate due to a...
The US Food and Drug Administration (FDA) has issued a Class II recall for combination extended-release capsules of dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, and amphetamine sulfate due to a...
The US Food and Drug...
07/09/2026
Pharmacy Learning Network

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