Pfizer Voluntary Nationwide Recalls Blood Pressure Medication Due to N-Nitroso-Quinapril Content

NEW YORK, NY.

Pfizer is voluntarily recalling five (5) lots of Accupril (Quinapril HCl) tablets distributed by Pfizer to the patient (consumer/user) level due to the presence of a nitrosamine, N-nitroso-quinapril, observed in recent testing above the Acceptable Daily Intake (ADI) level. 

Nitrosamines are common in water and foods, including cured and grilled meats, dairy products and vegetables. Everyone is exposed to some level of nitrosamines. These impurities may increase the risk of cancer if people are exposed to them above acceptable levels over long periods of time^.i 

Accupril is indicated for the treatment of hypertension, to lower blood pressure.  Accupril is also indicated in the management of heart failure as adjunctive therapy when added to conventional therapy including diuretics and/or digitalis. Accupril has a safety profile that has been established over 30 years. To date, Pfizer is not aware of reports of adverse events that have been assessed to be related to this recall. Pfizer believes the benefit/risk profile of the products remains positive based on currently available data. Although long-term ingestion of N-nitroso-quinapril may be associated with a potential increased cancer risk in humans, there is no immediate risk to patients taking this medication. Patients currently taking the products should consult with their doctor or health care provider about alternative treatment options for them.

The NDC, Lot Number, Expiration Date, and Configuration details for these products are indicated in the tables below and photos of the products can be found at the end of this press release. The product lots were distributed nationwide to wholesalers and distributors in the United States and Puerto Rico from December 2019 to April 2022.

Accupril® (Quinapril HCl Tablets), 10 mg
Accupril® (Quinapril HCl Tablets), 20 mg
Accupril® (Quinapril HCl Tablets), 40 mg

Pfizer places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Pfizer has notified direct consignees by letter to arrange for return of any recalled product.

Wholesalers and distributors with an existing inventory of the lots, listed in the table above, should stop use and distribution and quarantine the product immediately.

If you have further distributed the recalled product, please notify any accounts or additional locations which may have received the recalled product from you. Please conduct a sub-recall to those accounts and communicate this recall information immediately. Please request they immediately cease distribution of the affected product and promptly contact Sedgwick at 888-345-0481 (Mon.-Fri.8:00 am – 5:00 pm ET) to obtain a Business Reply Form (BRF) to initiate the return process.

If you received free product through the Pfizer Patient Assistance Program (PAP) or the Pfizer Institutional Patient Assistance Program (IPAP), please check your stock immediately against the table above. If you have any of the affected product lots in your inventory, please follow the instructions above for returning the product to Sedgwick. Additionally, if you are aware of any patients to whom you dispensed the affected lots who still may have the product in their possession, please ask them to return the product to you and then follow the instructions above for returning the product to Sedgwick. To request replacement product for any Pfizer PAP or Pfizer IPAP product you return, please contact 833-203-2776 (Mon.-Fri. 8 am-6 pm ET).

Patients who are taking this product should consult with their healthcare provider or pharmacy to determine if they have the affected product. Patients with the  affected product should contact Sedgwick at 888-345-0481 (Mon.-Fri. 8:00 am – 5:00 pm ET) for instructions on how to return their product and obtain reimbursement for their cost.

Healthcare Professionals with questions regarding this recall can contact Pfizer using the below information.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

•    Complete and submit the report Online
•    Regular Mail or Fax:  Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

References: https://www.fda.gov/drugs/drug-safety-and-availability/information-about-nitrosamine-impurities-medications

Source: Pfizer

• 
  Lo que necesita saber sobre el colesterol
  Mantenga el control para ayudar a prevenir enfermedades cardíacas, ataques cardíacos y accidentes cerebrovasculares (Características familiares) Comprender y mejorar el colesterol es importante para personas de todas las edades, incluidos niños y adolescentes. Tener niveles saludables de colesterol puede ayudar a mantener su corazón saludable y reducir sus posibilidades de contraer una enfermedad cardíaca o… Read more: Lo que necesita saber sobre el colesterol
• 
  The newly released Pfizer documents do not show that their COVID-19 vaccine is unsafe
  Fact Check By: Craig Jones, Newswise I’m sure it’ll be all over the mainstream news that Pfizer has now declared their COVID vaccines unsafe for pregnancy and breastfeeding after the government coerced and mandated thousands of pregnant women into having one. Claim Publisher and Date: Twitter on 2022-05-04 Beginning in late April, the Food and Drug Administration turned over… Read more: The newly released Pfizer documents do not show that their COVID-19 vaccine is unsafe
• 
  Groundbreaking Science Leads to FDA-Approved Treatment for Advanced Melanoma
  (Family Features) Despite preventative sun care measures like sunscreen and UV-protective clothing, skin cancer remains the most common cancer in the United States. In fact, rates of melanoma, a type of skin cancer, have been increasing steadily over the last 30 years. Melanoma can be mostly treatable when it is caught in its very early… Read more: Groundbreaking Science Leads to FDA-Approved Treatment for Advanced Melanoma
• 
  New study challenges stereotypes surrounding mental illness
  Some conditions are not always chronic and can still allow for one to thrive Newswise — TAMPA, Fla. – University of South Florida (USF) psychologists are challenging stereotypes surrounding mental illness – finding that some conditions are not always chronic and can still allow for one to thrive. In one of the broadest assessments yet… Read more: New study challenges stereotypes surrounding mental illness
• 
  PANCREATIC CANCER ACTION NETWORK HOSTS FIRST-EVER NATIONAL PANCAN PURPLESTRIDE, THE ULTIMATE EVENT TO END PANCREATIC CANCER
  Celebrities, Survivors, Caregivers, and Supporters Join Forces on One Big Day to Raise Awareness and Critical Funds for the World’s Toughest Cancer LOS ANGELES /PRNewswire/ — The Pancreatic Cancer Action Network (PanCAN) hosted its largest annual fundraiser, PanCAN PurpleStride, the ultimate event to end pancreatic cancer. For the first time ever in the organization’s history of PurpleStride fundraising events,… Read more: PANCREATIC CANCER ACTION NETWORK HOSTS FIRST-EVER NATIONAL PANCAN PURPLESTRIDE, THE ULTIMATE EVENT TO END PANCREATIC CANCER