Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0887-2015 — ACCU-CHEK Tender I 17/80 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.

U.S. FDA — Device Enforcement · United States · 2014-11-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0887-2015
Date of alert
2014-11-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Roche Diagnostics Operations, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04541448001
Reported risk: 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
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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