| Type of Product |
Medical Device |
| TGA Recall Reference |
RC-2014-RN-01036-1 |
| Product Name/Description |
Dimetapp Saline Nasal Drops for Infants
Batch numbers: 21320 & 21465
ARTG Number: 167019 |
| Recall Action Level |
Retail |
| Recall Action Classification |
Class II |
| Recall Action Commencement Date |
15/10/2014 |
| Responsible Entity |
|
| Reason/Issue |
Pfizer is recalling Dimetapp Saline Nasal Drops for Infants following a complaint received by TGA. The nature of the complaint involved the nozzle of the product becoming dislodged and subsequent flowing of the saline fluid onto a baby’s face. |
| Recall Action |
Recall |
| Recall Action Instructions |
Retailers and wholesalers are requested to inspect their stock and quarantine all units from the affected batches (21320 and 21465). Retailers are also requested to retain any units returned by consumers and provide a refund or replacement. This action has been closed-out on 18/07/2016. |
| Contact Information |
1800 502 790 - Pfizer Trade Operations |