The Medical Equipment Authority of the Ministry of Health would like to inform the public about the decision of the company Laboratoire de la Mer, for a precautionary recall of batch G239469 of the product PHYSIOMER BABY UNIDOSES.
Here is the relevant Notice issued by the company:
BATCH RECALL G239469 PHYSIOMER BABY UNIDOSES
Date: 22 / 04 / 2024
Dear Consumer,
As the responsible manufacturer of the medical device Physiomer Baby Unidoses, we have decided to conduct a voluntary recall of lot G239469 expiring 03/2027 and ONLY.
This is due to issues that appeared during the validation of the sterilization process, and which could theoretically lead to possible contamination of the product.
Despite the fact that no contamination has been detected in the product itself, respecting our customers and consumers and having as a permanent policy of our company the availability of high quality products, which fully and fully meet the consumer safety specifications in accordance with written provisions, we decided to proceed with the above voluntary recall.
The products included in it are identified by the batch number G239469 with an expiry of 03/2027 and were placed on the market between 06/03/2024-20/03/2024.
If you have product from the recalled lot, follow the steps below:
1. Stop using the product.
2. If you have questions about alternative therapies, you should contact a healthcare professional.
3. Return the unused or unopened product to the place of purchase.
The safety of our products is our first priority. If you have additional questions or need more information, please contact your Local Distributor CAPapaellinas Ltd on +357 22 741 741.
