File Photo: Pharmacy and Poisons Board banner. PHOTO|PPB
In Summary:
- PPB has recalled S-PRAZO capsules (Batch No. SPZ-302) due to a packaging error leading to mixed blister strips.
- Public and healthcare providers are advised to return the affected product and report any issues.
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The Pharmacy and Poisons Board (PPB) has stated that it is recalling S-PRAZO (Esomeprazole Magnesium Delayed-Release Capsules 40mg) Batch No. SPZ-302, manufactured by Laborate Pharmaceutical India Limited, following a market complaint regarding a packaging mix-up.
According to the PPB, some boxes were found to contain two different blister strips, including S-PRAZO Capsules and Donystatin Tablets, within the same outer carton.
“The product batch is being recalled following a market complaint regarding mix-up of blister strips; some boxes were found to contain two different blister strips, i.e. S-PRAZO Capsules and Donystatin Tablets, within the same outer carton,” read the statement in part.
The board urged health facilities, pharmaceutical outlets, and members of the public to stop using the capsules and return them to respective suppliers or the nearest healthcare facility.
“In view of the above, the Board advises all pharmaceutical outlets, healthcare facilities, healthcare professionals, and members of the public to stop further distribution, sale, issuing or use of the product batch and return the specified product batch to their nearest healthcare facility or respective suppliers,” PPB added.
Government Recalls Popular Ulcer Medication S-Prazo (Esomeprazole Magnesium Delayed-Release Capsules 40mg), Batch No. SPZ-302. PHOTO: PPB
The PPB also said it remains committed to protecting public health and encourages the public to report any suspected cases of sub-standard medicines or adverse drug reactions.
Reports can be made through the nearest healthcare facility or via the PPB’s website, email, mobile app, and USSD code.