"Food and Medicine" warns against the use of the needle "Tiroomo" and "Tiromu News"

The packaging is below the required manufacturing level, with holes on the packaging

The Food and Drug Administration (SFDA) has warned against the use of the Terumo Needle and Terumo Neolus Needle in a factory of the Terumo Company (Philippines) because the company has been using the Terumo needle and Terumo Neolus needle. plastic packaging of the needle is below the required manufacturing level. 1.5 mm, in addition to the holes on the packaging resulting from the needle head, which can lead to loss of product safety and contamination.

"The needle is described as an ultra-thin walled needle of 23 G x 1", 180707C and 180929C and NN + 2325R, a thin-walled needle 25G x 1, 180704C, NN + 2525R and 27G x 1 / Regular wall needle 2 ", operating number 181024C and NN + code 2713R.

The Commission informed health care providers of the manufacturer's call regarding the product and contacted the legal representative to take corrective action immediately, recommending users to check whether the product was affected by comparing the number of the product. 39; operation appearing on the product's cover with the warning data, stopping the product concerned and replacing it for free. By contacting the legal representative Abdulrahman Al-Gosaibi, "phone number 0112924219 – extension 183".

And invited consumers to report any incident or problem that may be associated with products, or any other device or medical product, through the Commission's Consolidated Call Center at 19999 or the National Center for Disease Control. Alert at https://ade.sfda.gov.sa/ Or the National Center for Medical Devices and Products Communications: https://ncmdr.sfda.gov.sa/ProblemReport.aspx.

---

The packaging is below the required manufacturing level, with holes on the packaging

The Food and Drug Administration (SFDA) has warned against the use of the Terumo Needle and Terumo Neolus Needle in a factory of the Terumo Company (Philippines) because the company has been using the Terumo needle and Terumo Neolus needle. plastic packaging of the needle is below the required manufacturing level. 1.5 mm, in addition to the holes on the packaging resulting from the needle head, which can lead to loss of product safety and contamination.

"The needle is described as an ultra-thin walled needle of 23 G x 1", 180707C and 180929C and NN + 2325R, a thin-walled needle 25G x 1, 180704C, NN + 2525R and 27G x 1 / Regular wall needle 2 ", operating number 181024C and NN + code 2713R.

The Commission informed health care providers of the manufacturer's call regarding the product and contacted the legal representative to take corrective action immediately, recommending users to check whether the product was affected by comparing the number of the product. 39; operation appearing on the product's cover with the warning data, stopping the product concerned and replacing it for free. By contacting the legal representative Abdulrahman Al-Gosaibi, "phone number 0112924219 – extension 183".

And invited consumers to report any incident or problem that may be associated with products, or any other device or medical product, through the Commission's Consolidated Call Center at 19999 or the National Center for Disease Control. Alert at https://ade.sfda.gov.sa/ Or the National Center for Medical Devices and Products Communications: https://ncmdr.sfda.gov.sa/ProblemReport.aspx.