Date Initiated by Firm | August 06, 2014 |
Date Posted | October 29, 2014 |
Recall Status1 |
Terminated 3 on April 29, 2015 |
Recall Number | Z-0145-2015 |
Recall Event ID |
69224 |
510(K)Number | K953673 |
Product Classification |
System, imaging, pulsed echo, ultrasonic - Product Code IYO
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Product | Parker Eclipse Probe Cover, Latex Free, REF 38-01, 10 Eclipse Probe Covers, Size: 2.37/1.75"W x 9.5"L (60/44 mm x 241 mm), Lot #D424, Expiry date 04/2016, Pre-gelled inside with Aquasonic 100 Ultrasound Transmission Gel
Product Usage: For use as a protective cover for medical ultrasound probes/transducers. |
Code Information |
Lot #D424, Part Number PM-038-0224E and BA-046-3801D 4/27/10 |
Recalling Firm/ Manufacturer |
Parker Laboratories, Inc. 286 Eldridge Road Fairfield NJ 07004-2509
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For Additional Information Contact | Ms. Kathleen Tirch 973-276-9500 Ext. 7142 |
Manufacturer Reason for Recall | Parker Laboratories, Inc. received a report of an incorrect expiration date on the inner boxes and on the plastic bags of the Eclipse Probe Covers. |
FDA Determined Cause 2 | Incorrect or no expiration date |
Action | Parker Laboratories Inc. sent an "Urgent Medical Device Product Recall" Letter/Response Form via Fedex to their customers. The letter indentified the affected product, problem and actions to be taken. For questions contact Parker Laboratories Quality Assurance at 973-276-9500, ext. 7142. |
Quantity in Commerce | 367 boxes |
Distribution | Worldwide Distribution: US (Nationwide) and country of: Canada. |
Total Product Life Cycle | TPLC Device Report |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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510(K) Database | 510(K)s with Product Code = IYO
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