Bi-Est Cream Recalled for Lack of Processing Control
The Medicine Shoppe Pharmacy is recalling Bi-Est cream due to lack of processing control. The product was distributed in Florida.
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. Per the rubric, FDA Class II recalls are assigned a severity score of 4 (Severe), particularly when specific injury reports are not explicitly detailed but the classification indicates a potential for temporary or medically reversible adverse health consequences.
Plain-English summary
The Medicine Shoppe Pharmacy in Port Charlotte, Florida, is recalling Bi-Est (50/50)/Progesterone/Testost 1.5/100/0.5 mg Cream 30 gm tube. The recall was initiated due to a lack of processing control. The affected product is a prescription cream with lot number 45132 and a discard-by date of 8/26/2020.
The recall is classified as FDA Class II. 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 pharmacist or healthcare provider for instructions on disposal or replacement.
The recalled product
- Product
- Bi-Est (50/50)/Progesterone/Testost 1.5/100/0.5 mg 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: 45132 Discard by: 8/26/2020
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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