Provepharm Recalls Phenylephrine Injection Over Contamination

January 25, 2025
1 min read
Representative Image. a person wearing gloves handling vials of medication or vaccines from a compartmentalized storage unit. Source - Pexels
Representative Image. a person wearing gloves handling vials of medication or vaccines from a compartmentalized storage unit. Source - Pexels

A dangerous discovery in a common emergency medicine has triggered an urgent nationwide recall. On January 24, 2025, Provepharm Inc. recalled its injectable blood pressure medication after finding black particles in sealed medicine vials.

The recall affects Phenylephrine Hydrochloride Injection, a medicine doctors use during surgery to help maintain stable blood pressure. Only one batch is affected – lot number 24020027, which expires in December 2025.

A box and a vial of Phenylephrine HCl Injection, USP . Source - FDA
A box and a vial of Phenylephrine HCl Injection, USP. Source – FDA

According to FDA warnings, particulate matter in injectable medicines can cause serious complications. These particles can travel through blood vessels and block blood flow to important organs like the heart or brain, potentially causing serious harm including stroke or death.


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This particular recall began after a pharmacy reported finding visible black particles in a single-sealed vial. The contaminated medicine was sent to hospitals and medical facilities across the country. While no one has reported getting sick from the medicine yet, wholesalers, distributors, compounding companies and hospitals must immediately cease use and return the product.

Healthcare workers can identify the recalled medicine by checking:

  • The ID number (called NDC): 81284-213-01
  • Lot number: 24020027
  • Expiration date: December 2025
  • Size: 10 mL single-dose vial

Provepharm is working with a company called Sedgwick to collect all unused vials. Hospitals should send recalled medicine to:

Sedgwick

Event## 8664

2670 Executive Drive, Suite A

Indianapolis, IN 46241

Anyone who thinks they might have had a bad reaction to this medicine should tell their doctor right away. Doctors and patients can report problems to the FDA by:

  • Going online to the MedWatch program
  • Calling 1-800-332-1088
  • Asking for a form by mail

For questions about returning the medicine, contact Sedgwick at 866-737-5394 or email [email protected].

This recall highlights why strict quality checks are crucial when making injectable medicines. Even tiny particles can cause serious harm when injected directly into the bloodstream.

Tejal Somvanshi

Meet Tejal Somvanshi, a soulful wanderer and a staunch wellness advocate, who elegantly navigates through the enchanting domains of Fashion and Beauty with a natural panache. Her journey, vividly painted with hues from a vibrant past in the media production world, empowers her to carve out stories that slice through the cacophony, where brands morph into characters and marketing gimmicks evolve into intriguing plot twists. To Tejal, travel is not merely an activity; it unfolds as a chapter brimming with adventures and serendipitous tales, while health is not just a regimen but a steadfast companion in her everyday epic. In the realms of fashion and beauty, she discovers her muse, weaving a narrative where each style narrates a story, and every beauty trend sparks a dialogue. Tejal seamlessly melds the spontaneous spirit of the media industry with the eloquent prose of a storyteller, crafting tales as vibrant and dynamic as the industry she thrives in.

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