| Class 2 Device Recall UCHRAP or Universal Compact Head Ring Adapter Plate | |
Date Initiated by Firm | August 21, 2015 |
Date Posted | October 06, 2015 |
Recall Status1 |
Terminated 3 on October 13, 2016 |
Recall Number | Z-0025-2016 |
Recall Event ID |
72068 |
510(K)Number | K944463 |
Product Classification |
Neurological stereotaxic Instrument - Product Code HAW
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Product | Universal Compact Head Ring Adapter Plate (UCHRAP), a component of the Universal Compact Head Ring Adapter, UCHRA. The UCHRA is a component of the Integra CRW Precision Arc Stereotactic System. |
Code Information |
Cat. No. UCHRAP; Serial No.s 900, 901, 902, 904, 905, 906 |
Recalling Firm/ Manufacturer |
Integra LifeSciences Corp. 311 Enterprise Dr Plainsboro NJ 08536-3344
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For Additional Information Contact | Mr. David E. Gronostajski 609-936-6822 |
Manufacturer Reason for Recall | Integra identified that the UCHRAP component (Arc Adapter Plate) would not assemble properly to the UCHRAR component (ARC Adapter Ring) of the Compact Head Ring Adapter due to an error in the manufacturing drawing. |
FDA Determined Cause 2 | Process design |
Action | Integra sent an Urgent-Voluntary Medical Device Recall letter dated August 19, 2015, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.
The firm instructed their customers to:
1. Review your inventory and determine if you have an UCHRAP Adapter Plate with an affected serial number listed on the next page. If you do not, it is not affected and you can continue to use it.
2. If you do have product with a serial number listed on the next page, stop using it immediately and remove it from service.
3. Complete the attached form. If you do not have product with a serial number listed, check the box, I do not have any product with a serial number on the list below.
4. If you do have product with a serial number listed, check the box, I do have product(s) with a serial number below. Circle the lot numbers and record the total quantity of all lot numbers you have.
5. Complete the other information and return it by email or fax as indicated on the form or by providing it to your Integra Neuro Specialist.
If an Integra Neuro Specialist has not already done so, Customer Service will contact you and provide an RMA number and directions for returning and replacing the product. Should you have any questions regarding these instructions, please call : (513) 533-7932. For any other questions, please call (609) 936-6822. |
Quantity in Commerce | 6 units |
Distribution | Worldwide Distribution - US Distribution to the states of : NJ, TX and WY., and to the countries of : Algeria, Germany and India. |
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 = HAW
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