Pharm D Solutions Recalls Epi-Shugarcaine Kit Due to Sterility Concerns
Pharm D Solutions is recalling 70 bottles of Epi-Shugarcaine Kit Solution because the company cannot ensure the product is sterile.
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, which corresponds to a Severe severity score under the rubric for potential serious, reversible health consequences.
Plain-English summary
Pharm D Solutions, LLC is recalling 70 bottles of Epi-Shugarcaine Kit Solution (NDC 69699-1409-60). The recall was initiated because the company lacks assurance of the product's sterility.
The affected product was distributed nationwide. The specific lot code is 08272018:79, with a discard-by date of October 1, 2018.
Consumers and healthcare providers should stop using the recalled product and contact Pharm D Solutions for further instructions or a refund.
The recalled product
- Product
- Epi-Shugarcaine Kit Solution Pharm D Solutions, Houston, Texas --- NDC 69699-1409-60
- Manufacturer
- Pharm D Solutions, LLC
- Category
- Drug — Injectable Solution
- Affected units
- 70
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)
- 08272018:79 Discard by: 10/1/2018
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 79 recalled by Pharm D Solutions, LLC 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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