NAFDAC
The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from the UK Medicines and Healthcare Products Regulatory Agency (MHRA) that Takeda UK Limited is recalling Instanyl 100mcg nasal spray solution batch Number 447055. The recall is due to the observation of cracked vials during inspection of the bulk vials and release testing of the finished products.
So far, the company has not received any reports of damage for the marketed products. However, the batch is being recalled as a precautionary measure due to the low potential for breaking or cracking of the glass vial, which is contained within the plastic actuator casing and a potential risk of microbial contamination.
Instanyl is indicated for the management of breakthrough pain in adults already receiving maintenance opioid therapy for chronic cancer pain. Breakthrough pain is a transitory exacerbation of pain that occurs on a background of otherwise controlled persistent pain.
The details of the affected product are as follows:
| Product | Company Name | Batch number | Expiry Date | Pack Size | First Distributed |
| Instanyl 100mcg Nasal Spray | Takeda UK Limited | 447055 | 31/10/2021 | 1 x 6 single dose containers | 14/04/2020 |
Healthcare providers are encouraged to:
Healthcare professionals are encouraged to report any adverse events or side effects related to the use of this product to the nearest NAFDAC office, NAFDAC PRASCOR (20543 TOLL FREE from all networks), or via pharmacovigilance@nafdac.gov.ng
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