Bella Pharmaceuticals Recalls MIC 25/50/50 Vials Due to Sterility Concerns
Bella Pharmaceuticals is recalling MIC 25/50/50 vials because the company cannot ensure the product is sterile. The recall affects 5 vials distributed nationwide.
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 the hazard involves a lack of assurance of sterility, which poses a significant risk of serious injury or infection, meeting the criteria for a Severe rating.
Plain-English summary
Bella Pharmaceuticals, Inc. is recalling MIC 25/50/50, 30mL vials, which are prescription-only medications. The recall is being conducted because the company lacks assurance of the product's sterility.
The affected product consists of 5 vials with Lot # BPMIC30072917 and an expiration date of 1/29/18. These vials were distributed nationwide within the United States.
Consumers and healthcare providers should stop using the recalled product and contact Bella Pharmaceuticals at 1 (877) BELLA for further instructions.
The recalled product
- Product
- MIC 25/50/50, 30mL vials, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.
- Manufacturer
- Bella Pharmaceuticals, Inc.
- Category
- Drug — Injectable Medication
- Affected units
- 5
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 (2)
- Lot #: BPMIC30072917
- Exp. 1/29/18
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 16 recalled by Bella Pharmaceuticals, Inc. 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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