Pallimed Recalls Diazepam Injectable Due to Sterility Assurance Concerns
Pallimed Solutions is recalling Diazepam Injectable vials because FDA inspections raised concerns about quality control procedures that impacted sterility assurance.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II and involves a lack of assurance of sterility in an injectable drug, which poses a risk of serious injury or death from infection, fitting the 'Severe' criteria for significant injury reports or high-risk defects.
Plain-English summary
Pallimed Solutions Pharmacy in Woburn, Massachusetts, is recalling Diazepam Injectable. The recall involves 7 vials of the compounded medication. The distribution pattern is listed as nationwide, and the recall covers all lots within their expiry dates.
The recall was initiated due to a lack of assurance of sterility. FDA inspectional findings resulted in concerns associated with quality control procedures that impacted sterility assurance. The agency has classified this recall as Class II.
Consumers and healthcare providers should stop using the affected Diazepam Injectable vials and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- Diazepam Injectable, compounded by Pallimed Solutions Pharmacy, Woburn, MA
- Manufacturer
- Pallimed Solutions
- Category
- Drug — Injectable
- Affected units
- 7
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All lots within expiry
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 25 recalled by Pallimed Solutions under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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