Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is recalling its P-211-M1 and...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact TZ Medical Inc. directly.
Affected Products
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.
Quantity: US: 10,410 pieces; Outside US: 100 pieces
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About TZ Medical Inc.
TZ Medical Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report