Well Care Compounding Pharmacy Recalls QUAD-MIX #2 Due to Sterility Concerns
Well Care Compounding Pharmacy is recalling QUAD-MIX #2 vials due to FDA inspection findings of GMP violations that may impact sterility.
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 agency classification is FDA Class II, and the hazard involves a lack of assurance of sterility in a medical product, which aligns with the 'Severe' criteria for significant potential harm.
Plain-English summary
Well Care Compounding Pharmacy in Las Vegas, Nevada, is recalling QUAD-MIX #2, a prescription-only medication packaged in 5mL vials. The recall involves 869 units distributed in Nevada.
The recall was initiated because an FDA inspection identified Good Manufacturing Practice (GMP) violations that potentially impact the product's quality and sterility. The source text does not report any specific illnesses or injuries associated with the product.
Consumers who have this product should stop using it and contact their healthcare provider or the pharmacy for instructions on how to return or dispose of the medication.
The recalled product
- Product
- QUAD-MIX #2, packaged in 5mL vial, Rx only, Well Care Compounding Pharmacy Las Vegas, NV 89121
- Manufacturer
- Well Care Compounding Pharmacy
- Category
- Drug — Compounded Prescription
- Hazard
- Affected units
- 869
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 (4)
- Lot #: 02172016:86@12
- Exp.05/18/2016
- Lot #: 04012016:22@4
- Exp.06/30/2016
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 51 recalled by Well Care Compounding Pharmacy 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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