Ketoprofen/DMSO Lipoderm Recalled for Lack of Processing Control
The Medicine Shoppe Pharmacy is recalling Ketoprofen/DMSO 20%/10% Lipoderm 50 gm jars due to lack of processing control.
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, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
The Medicine Shoppe Pharmacy in Port Charlotte, Florida, is recalling Ketoprofen/DMSO 20%/10% Lipoderm 50 gm jars. The recall was initiated due to a lack of processing control. The affected product is a prescription medication distributed in Florida.
The specific lot number is 44552, and the discard-by date is March 23, 2020. The product is a 50 gm jar. 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
- Ketoprofen/DMSO 20%/10% Lipoderm 50 gm jar, Rx, The Medicine Shoppe Pharmacy, Port Charlotte, FL
- Manufacturer
- The Medicine Shoppe Pharmacy
- Category
- Drug — Topical Analgesic
- 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: 44552 Discard by: 3/23/2020
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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