Bi-Est Cream Recalled for Lack of Processing Control
The Medicine Shoppe Pharmacy is recalling Bi-Est 8:2/Progesterone cream due to lack of processing control. The product was distributed in Florida.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity level when no serious injury or death is reported. The hazard is a processing control issue without reported adverse health consequences.
Plain-English summary
The Medicine Shoppe Pharmacy in Port Charlotte, Florida, is recalling Bi-Est 8:2/Progesterone 2.5 mg/150/mL Cream 30 gm tubes. The recall is due to a lack of processing control. The affected product is a prescription cream with lot number 44908 and a discard-by date of 6/17/2020.
The recall is classified as Class II by the U.S. Food and Drug Administration. The product was distributed in Florida. No specific illnesses or injuries are reported in the source text.
Consumers should stop using the product and contact their healthcare provider or the pharmacy for further instructions.
The recalled product
- Product
- Bi-Est 8:2/Progesterone 2.5 mg/150/mL Cream 30 gm tube, Rx, The Medicine Shoppe Pharmacy, Port Charlotte, FL
- Manufacturer
- The Medicine Shoppe Pharmacy
- Category
- Drug — Topical Cream
- Hazard
- Affected units
- 1
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)
- Lot: 44908 Discard by: 6/17/2020
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 54 recalled by The Medicine Shoppe 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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