Assurance Infusion Recalls BUP/HYDROM/SUF Injection Due to Sterility Concerns
Assurance Infusion is recalling 2 syringes of BUP 5MG/HYDROM 15MG/SUF 600MCG/ML injection due to a lack of 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. According to the rubric, FDA Class II recalls with potential for significant injury (such as lack of sterility assurance in injectable drugs) are classified as Severe.
Plain-English summary
Assurance Infusion is recalling 2 syringes of BUP 5MG/HYDROM 15MG/SUF 600MCG/ML (40ML) INJ in 20 mL syringe. The recall is due to a lack of sterility assurance. The affected product is identified by Lot 12102019@6 with an expiration date of 12/19/2019.
The product was distributed nationwide within the United States. The source text does not specify the number of units distributed or report any illnesses or injuries associated with the product.
Consumers and healthcare providers should stop using the affected product and contact Assurance Infusion at (713) 533-8800 for further instructions.
The recalled product
- Product
- BUP 5MG/ HYDROM 15MG/ SUF 600MCG/ML (40ML) INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Manufacturer
- Assurance Infusion
- Category
- Drug — Injectable
- Hazard
- Affected units
- 2
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)
- Lots: 12102019@6 Exp. 12/19/2019
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 118 recalled by Assurance Infusion 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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