Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Medicine |
| Medsafe Reference: | 14190 |
| Brand Name: | Albuterex Xtreme (fat loss product) |
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| Recalling Organisation: | |
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| Manufacturer: | |
| Brand Name: | Albutarex Xtreme (fat loss product) |
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| Affected: | 190186MN |
| Recalling Organisation: | Nutrition Systems NZ Pty Ltd 213b John F Kennedy Drive Palmerston North 4144 |
| Contact Information: | |
| Manufacturer: | |
| Brand Name: | Albuterex Femme Formula (fat loss product) |
| Dose Form/Strength: | |
| Affected: | |
| Recalling Organisation: | |
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| Manufacturer: | |
| Issue: | The Therapeutic Goods Administration received advice of a possible adverse reaction to a product identified as 'Albuterex Xtreme Formula'. The TGA subsequently conducted analysis of a sample of this product. The product was found to contain high levels of caffeine as well as quantities of yohimbine and theophylline none of which are declared on the label of the product. |
| Recall action type: | Recall - Unapproved medicine |
| Recall action: | Recall |
| Level of recall: | Retail |
| Date Commenced: | 26/2/2013 |





