Product Recall: Modified Fluid Gelatin 4% Injection (Infusol SG)
Post date: Nov 04, 2019 5:4:20 AM
24th October 2019 (Circular No. SP PPUM: 447/2019):
Please be informed that Ain Medicare Sdn Bhd, the distributor of this product, has been given notice of product recall for the particular batch number P390A262 due to failure to pass bacterial endotoxin test. The use of this product should be stopped immediately.
Therefore, all clinical areas keeping the stocks for this product are required to do prompt checking on the batch number of the current stocks. Kindly segregate the affected stocks according to the batch number and send to Inpatient Pharmacy for exchange of stocks.