[pending] LIDOLOG KIT (LIDOCAINE, KENALOG, POVIDONE IODINE)
Pending LLM rewrite. Source: FDA_DRUG D-0552-2026.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Pending LLM scoring against the rubric.
Plain-English summary
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
The recalled product
- Product
- LIDOLOG KIT (LIDOCAINE, KENALOG, POVIDONE IODINE)
- Brand
- LIDOLOG KIT
- Manufacturer
- Eugia US LLC
- Category
- Drug — Drugs
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 (5)
- Lot
- expiry: Lot 3LC26029A
- exp Feb-2029
- Lot 3LC26031A
- exp Mar-2029
Distribution
Distributed nationwide across the United States.
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