| Class 2 Device Recall ROTEM extem (for use on ROTEM delta instrument) | |
Date Initiated by Firm | July 23, 2019 |
Create Date | September 06, 2019 |
Recall Status1 |
Terminated 3 on April 27, 2020 |
Recall Number | Z-2486-2019 |
Recall Event ID |
83523 |
510(K)Number | K101533 |
Product Classification |
System, multipurpose for in vitro coagulation studies - Product Code JPA
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Product | ROTEM ex-tem
Canada Part No: 503-05-CA |
Code Information |
Lot # : 42255801 (Canada) |
Recalling Firm/ Manufacturer |
Instrumentation Laboratory Co. 180 Hartwell Rd Bedford MA 01730-2443
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For Additional Information Contact | PBM Technical Support Center 800-678-0710 |
Manufacturer Reason for Recall | Prolonged clotting times |
FDA Determined Cause 2 | Nonconforming Material/Component |
Action | -Check your inventory for Lot No. 42255901 / 42255801 and destroy all remaining material.
- Document the destruction on the Mandatory Tracking Response Record and return the completed and signed form to the fax number or e-mail address listed on the next page.
-Contact your local representative for an alternative product lot of ROTEM ex-tem, Part No. 503-05-US / 503-05-CA.
-Share this information with your laboratory staff and follow your internal procedures.
-Forward this notification to all affected locations within your facility.
-Retain a copy of this notification for your records.
-Return the completed and signed form confirming lot destruction and quantities to: FAX No. 781-861-4207 or Email: ra-usa@ilww.com
For Technical Questions: Call ROTEM PBM Technical Support Center at 1-800-678-0710, Option # 4
For Replacement Lot: Call IL Customer Service Center at 1-800-955-9525, Option # 0 |
Quantity in Commerce | 44 kits |
Distribution | States:
IL
WI
MI
Canada, Spain, Portugal, Poland, Italy, Israel, Switzerland, Denmark, Kazakhstan, United Kingdom, Germany, Netherlands, Belgium, France, Jordan, India, Hong Kong, Austria, Czechia, Australia, Sri Lanka, Argentina, Vietnam, Singapore, Japan, South Korea, Cyprus, Ireland, Hungary, Sweden, Serbia. |
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 = JPA
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