FDA Recall Terminated

adult defibrillation, cardioversion, pacing, monitoring Disposable Electrodes, Model P-211-M1 and P-214-M1. Product Usage: Used by trained professionals in hospitals, doctors offices, and Emergency Medical Services for adult low-energy defibrillation, transcutaneous pacing, cardioversion and monitoring.

Recall: Z-1438-2013 · Initiated April 30, 2013

Recall

Recall Number
Z-1438-2013
Event Number
65120
Firm
TZ Medical Inc.
FEI Number
1000127185
Product Code
DRO
Status
Terminated
Root Cause
Process control
Initiated
April 30, 2013
Posted
May 30, 2013
Terminated
September 5, 2013
Address
17750 SW Upper Boones Ferry Rd, Ste 150, Portland, OR, 97224-7086

Description

adult defibrillation, cardioversion, pacing, monitoring Disposable Electrodes, Model P-211-M1 and P-214-M1. Product Usage: Used by trained professionals in hospitals, doctors offices, and Emergency Medical Services for adult low-energy defibrillation, transcutaneous pacing, cardioversion and monitoring.

Reason

TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio Control Compatible transparent defibrillation electrodes because it may contain a defective white wire on the connector assembly. If a failure were to occur, the end user would be able to identify the failure by inspecting the white wire 1/4 inch from the Gray Medtronic / Physio adapter. The consignees will notice discolor

Action

TZ Medical Inc. started notifying their customers by telephone on April 30, 2013. The firm followed up with an Urgent: Medical Device Recall notification letter dated May 14, 2013, to their consignees. TZ Medical Inc., Representatives have will contact all affected customers and arrange for the replacement of the effected product in stock with inspected product. For any questions about this recall, please fax to 503-639-0239.

Distribution

Worldwide distribution - USA (nationwide) and Chile.

Quantity

US: 10,410 pieces; Outside US: 100 pieces