Gentamicin Injection BP 80 mg in 2 mL Steriluer ampoules in packs of 10 or 50
Potential allergic reaction - affected batches of Gentamicin Injection may contain higher than expected amounts of histamine.
9 product recalls were published during this week. Review the summaries below, then follow the official source before taking action.
Potential allergic reaction - affected batches of Gentamicin Injection may contain higher than expected amounts of histamine.
In certain cases, the handlebars have not been properly manufactured and will bend easily in normal use.
Recall for product correction (firmware update) These devices may be operating outside their permissible frequency band (915-928 MHz) and may cause interference with mobile towers (operating in the 902-915 MHz frequency band). This potential interference does not cause any interruption to the Surflink Media and Surflink Media 2 devices and the will continue to function correctly. What consumers should do Users are being asked to temporarily return their devices to Starkey Hearing Technologies so they can undertake a firmware update to correct this issue. Updated devices will only operate within the permissible 915-928 MHz frequency band. If you or someone you care for uses a Surflink Media or Surflink Media 2 device, you should receive further information about this issue from Starkey Hearing Technologies, as well as a form to fill in and a prepaid bag to return the device. Alternatively, you can choose to return the device to the audiology clinic where you purchased it. Once the firmware has been updated, the device will be returned to you or the audiology clinic where you purchased it, so that it can be returned to you. For further information, talk to your audiology clinic or contact Starkey Hearing Technologies on 1800 024 985.
The circumference of the leg of the sleep shorts does not comply with the measurement requirements of the mandatory standard 'Consumer Goods (Children’s Nightwear and Limited Daywear and Paper Patterns for Children’s Nightwear) Safety Standard 2017'.
The jelly cups contain konjac. Jelly cups containing konjac are permanently banned in Australia.
The jelly cups contain konjac. Jelly cups containing konjac are permanently banned in Australia.
Sale of betel nuts is prohibited.
Potential for incomplete delivery of medication. The batch is being recalled due to reports of the active ingredient powder not dissolving sufficiently with the diluent liquid in the syringe, causing clumping. The clumping is readily visible to the naked eye in affected products and should be noticed on inspection.
The presence of an undeclared allergen (fish).