ACCU-CHEK Tender II 13/80 10 + 10 pieces Product Usage: Intended for the infusion and/or injection of fluids into the body below the surface of the skin. The indwelling catheter can be inserted independently from the infusion catheter and can be accessed for the injections through the injection port
Check against the official notice below — it lists the full affected range.
Roche Diagnostics Operations, Inc. is recalling ACCU-CHEK Tender II 13/80 10 + 10 piece infusion sets used to deliver insulin into the body. The manufacturer UnoMedical identified a potential defect where the tubing could become detached at the connection point on these infusion sets. If the tubing detaches, insulin delivery stops, but the pump will not alarm to alert the user that the delivery has been interrupted.
The recall affects 13,041 boxes distributed nationwide in the United States. The affected products have catalog number 04541472001 and lot numbers 5053291 and 5078661. The source document does not specify a remedy or actions consumers should take.
Written by software from the official notice below. Not reviewed by a lawyer.
Roche Diabetes Care was informed by UnoMedical, the Manufacturer of ACCU-CHEK Tender I and ACCU-CHEK Tender II infusion sets, about potential for the the tubing of the infusion set to become detached at the connect/disconnect location on the ACCU-CHEK Tender I and ACCU-CHEK Tender II infusion sets. If tubing detachment occurs, insulin delivery is interrupted and the pump will not alarm to notify
Reason for recall: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of ACCU-CHEK Tender I and ACCU-CHEK Tender II infusion sets, about potential for the the tubing of the infusion set to become detached at the connect/disconnect location on the ACCU-CHEK Tender I and ACCU-CHEK Tender II infusion sets. If tubing detachment occurs, insulin delivery is interrupted and the pump will not alarm to notify Distribution: US Nationwide Distribution Quantity: Total of 13,041 boxes Lot/code info: Catalog: 04541472001 and lots: 5053291 and 5078661.
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.