Theracare Maximum Strength Pain Relief 4% Lidocaine recall: CGMP Deviations
THERACARE MAXIMUM STRENGTH PAIN RELIEF 4% LIDOCAINE PATCH, a) 1 patch (NDC 71101-001-24, UPC 8 45717 00878 5) and b) 6 patches (NDC 71101-001-06, UPC…
Why was Theracare Maximum Strength Pain Relief 4% Lidocaine recalled?
cGMP Deviations
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
a) UPC 8 45717 00878 5 b) UPC 8 45717 01056 6
- Product
- THERACARE MAXIMUM STRENGTH PAIN RELIEF 4% LIDOCAINE PATCH, a) 1 patch (NDC 71101-001-24, UPC 8 45717 00878 5) and b) 6 patches (NDC 71101-001-06, UPC…
- Recalling firm
- Unexo Life Sciences Private Limited
- Quantity
- 455,536 patches
- Distribution
- Nationwide in the US
- Recall date
- December 4, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)