FDAClass IIIMay 2, 2018

Diltiazem HCl Extended-Release Capsules recall: Failed Dissolution

Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY…

Why was Diltiazem HCl Extended-Release Capsules recalled?

Failed Dissolution Specifications. High dissolution results were obtained 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?

Lot #: 0115087, Exp. 12/2018

Product
Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY…
Recalling firm
Mckesson Packaging Services
Quantity
2966 cartons
Distribution
Nationwide with the US
Recall date
May 2, 2018
Classification
Class III
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls