Glimepiride Tablets recall
GLIMEPIRIDE TABLETS, USP 2 mg, a)100 count bottle, (NDC 42571-101-01), b) 500 count Bottle (NDC 42571-101-05), Rx only, Manufactured by: Micro Labs…
Why was Glimepiride Tablets recalled?
Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.
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?
GLBG001 Exp.12/14, GLBG008 Exp. 06/15
- Product
- GLIMEPIRIDE TABLETS, USP 2 mg, a)100 count bottle, (NDC 42571-101-01), b) 500 count Bottle (NDC 42571-101-05), Rx only, Manufactured by: Micro Labs…
- Recalling firm
- Micro Labs Usa, Inc S
- Quantity
- 11,328 bottles
- Distribution
- CT, FL, MD, MS, NY
- Recall date
- November 5, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)