FDAClass IIIOctober 18, 2017

Mobic (meloxicam) tablets recall: Labeling Error

Mobic (meloxicam) tablets, 15 mg, package in 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT…

Why was Mobic (meloxicam) tablets recalled?

Labeling: Incorrect or missing package insert. One lot of Mobic Tablets is packaged with an incorrect insert.

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?

Lot 754037

Product
Mobic (meloxicam) tablets, 15 mg, package in 100-count bottle, Rx only, Dist. by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT…
Recalling firm
Boehringer Ingelheim Pharmaceuticals, Inc.
Quantity
128 bottles
Distribution
CO, OH
Recall date
October 18, 2017
Classification
Class III
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls