Recall Z-1372-2011
Heart Sync, Inc · initiated December 17, 2010
Product
Medstorm Adult Radiolucent Zoll Medical (Part # 16381, HeartSync, Ann Arbor, MI. The Adult Radiolucent Multifunction Tin Electrodes are indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single patient use only. The electrodes provide the conductive interface between the defibrillator and/or the external transcutaneous cardiac pacemaker and the patients skin. When a patient requires defibrillation, cardioversion or external pacing, these electrodes will be applied to the patient and connected to the respective low power mono-phasic or bi-phasic defibrillator (360 joules maximum) or external pacemaker.
Codes / lots: Lot # Y032709-1
Reason for recall
The seal on the electrode pouch may be open, exposing the electrode to the outside environment. The package does have a caution statement that states, " Do not open package until immediately prior to using electrodes. and Electrodes may dry out when removed from packaging and exposed to air.
FDA-determined cause: Packaging
Action taken
Heart Sync, Inc sent an URGENT MEDICAL DEVICE RECALL letter dated December 23, 2010, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to: Examine their inventory and quarantine product that was subject to the recall that was not sealed properly. Contact any customers if they further distributed the product and notify them at once of this product recall. Contact the firm if they had any unused product. The firm would issue a UPS Call Tag to have the product returned to them and the firm would send replacement product as soon as they were notified. Complete and return the Recall Return Response Form to the firm in the attached prepaid envelope. For any questions regarding this recall call 734-213-5530.
Details
- Recall number
- Z-1372-2011
- Initiated
- December 17, 2010
- Posted by FDA
- February 18, 2011
- Terminated
- July 13, 2011
- Product code
- MLN – Electrode, Electrocardiograph, Multi-Function
- Quantity
- 300
- Distribution
- Worldwide Distribution - USA including AK, AZ, CA, FL, IL, KS, LA, MA, ND, NM, OH, TX, WA, WI and WV; and Canada
- Recalling firm
- Heart Sync, Inc, Ann Arbor, MI
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-1371-2011 | Medstorm Adult Radiolucent Electrode Philips Medical , Part #16250, HeartSync Ann Arbor…The seal on the electrode pouch may be open, exposing the electrode to the outside environment. The package… | 12/17/2010Terminated |