Reported Jun 5, 2013 · Terminated
Vermed, Inc Radiotransparent Defibrillation Electrodes Monophasic or biphasic compatible…
Heart Sync, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Heart Sync, Inc · 5643 Plymouth Rd · Ann Arbor, MI · 48105-9586
Is this the product you have?
- Vermed, Inc Radiotransparent Defibrillation Electrodes Monophasic or biphasic compatible defibrillation/cardioversion/pacing/ECG Monitoring electrodes. Used in connection with a defibrillator to deliver an electrical current (shock) to the patient's heart during cardiac emergencies.
- Lot codes and dates
- Part NumberD304
- and lot numbers
Y100112-02Y102212-03Y121312-18Y012413-02Y022013-01Y032113-01
- Amount recalled
- 17180 units for all part numbers
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
On 4/18/13 HEARTSYNC became aware of a recall from their wire/connector sub-assembly supplier which is used in the C100-Physio Electrodes. There were reports of equipment damage due to misalignment from tooling installed in August 2012. The result of this damage could render the device incapable of delivering the appropriate energy or shock to the patient.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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