Methocarbamol recall: CGMP Deviations
Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 g container (NDC…
Why was Methocarbamol recalled?
CGMP Deviations: Lack of quality assurance at the API manufacturer.
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?
Lots: MCMR1308029NS, MCMR1308029NS-4202015; Exp. 08/18
- Product
- Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 g container (NDC…
- Recalling firm
- American Pharmaceutical Ingredients LLC
- Quantity
- 5,000g (5 kg)
- Distribution
- Nationwide
- Recall date
- July 12, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)