Safety Alerts & Recalls

What does this mean?

This recall for Nifedipine extended-release 90 mg tablets from Greenstone LLC was issued at a warehouse and pharmacy level only. The FDA and the manufacturer have determined that any recalled product that may have been dispensed to patients does not pose a significant health risk. If you have blisterpacks of Nifedipine extended-release 90mg tablets labeled with the lot number V11079 and are concerned, you should speak to your doctor.

Greenstone LLC Recalls Single Lot of Nifedipine, Extended-Release 90 mg Tablets

Greenstone LLC has recalled a single lot of Nifedipine, extended-release 90 mg tablets packaged in blister packs. Lot number V110079 has been recalled because an incorrect expiration date was printed on the label.

Nifedipine is used in the treatment of high blood pressure. This recall alert only applies to the single lot of the generic Nifedipine, extended-release 90mg tablets in blister packs distributed by Greenstone LLC. No other Nifedipine products were involved in this recall.

To view the FDA notice about this recall, please visit: more information here

Source: FDA
Publication Date: 2014-02-04
Last Updated: 2014-02-07

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