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Cayman: FDA recall – Ranitidine Products

Zantac

From Health Services Authority

Please be advised, The FDA has ordered a recall of all Ranitidine products, due to manufacturing issues.

Patients taking any form of prescription Ranitidine (tablets or liquids) have been asked to discontinue and contact their doctor for an alternative.

Persons have also been advised not to purchase over-the-counter Ranitidine products (e.g. Zantac®).

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