Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 22075 |
| Brand Name: | Dimetapp Cough Cold & Flu Daytime/Nightime |
| Dose Form/Strength: | Capsule . |
| Affected: | E8895, F1453 |
| Recalling Organisation: | Pfizer New Zealand Limited C/-ICON Clinical Research New Zealand Ltd Plaza Level, c/-Regus 41 Shortland Street AUCKLAND 1010 |
| Contact Information: | 0800 734 076 |
| Manufacturer: | Catalent Australia Pty Ltd |
| Issue: | Pfizer Australia has received a complaint of incorrect sequencing of Dimetapp Daytime/Nightime Liquid Caps with the night variant in the morning section and the day variant in the bedtime section of the blister platform. |
| Recall action type: | Recall |
| Recall action: | Recall |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 12/10/2017 |
