| Date Initiated by Firm |
January 06, 2016 |
| Date Posted |
February 24, 2016 |
| Recall Status1 |
Terminated 3 on August 23, 2017 |
| Recall Number |
Z-0802-2016 |
| Recall Event ID |
73056 |
| Product Classification |
Catheter, percutaneous - Product Code DQY
|
| Product |
Radial Artery Pressure Monitoring Catheter Sets and Trays
The subject sets and trays are comprised of a single-lumen uncoated or heparin-coated catheter. Product catalog numbers with heparin coating are designated by the suffix BH. |
| Code Information |
RPN/Catalog number: C-PMS-250-RA C-PMS-251-RA C-PMS-300-RA C-PMS-300-RA-CHOP C-PMS-301J-RA C-PMS-301-RA C-PMS-400-RA C-PMSY-250-RA C-PMSY-300-RA C-PMSY-301-RA Lots: 6049998 6160195 6160212 NS5898558 NS6063328 NS6178204 NS6178206 5895605 6191185 5793196 5800313 5800443 5800569 5806981 5810905 5810917 5824484 5824546 5824547 5824548 5866984 5866985 5866986 5870319 5881447 5881519 5889496 5891905 5911486 5922847 5922848 5925742 5928632 5939446 5939447 5939448 5976502 6025016 6025094 6033768 6034981 6034983 6050000 6062738 6062742 6067675 6067676 6075206 6075207 6083936 6083954 6083985 6083986 6129056 6148790 6160236 6165591 6174974 6175289 6191362 6269150 NS6063331 NS6108226 NS6170739 NS6170767 5905252 6003109 NS6072553 5793197 5800571 5800572 5824485 5824551 5845063 5864072 5866988 5873125 5881151 5881152 5884641 5884642 5889464 5892063 5892064 5922850 5939431 5942091 5951549 5953768 5954322 5967404 5974281 5994817 5996926 6003161 6003162 6017048 6025095 6025145 6034984 6042699 6050002 6075210 6075211 6075212 6081723 6083988 6100756 6124809 6125111 6148791 6153122 6160239 6160240 6168131 6171368 6187477 6250532 6059759 NS6047396 NS6047397 NS6047398 NS6047399 NS6047440 NS6047442 6124812 5793192 5824526 5884647 5892068 5942090 5967410 6003167 6059765 6134128 6153124 6168137 6254068 5793193 5866995 5892069 5942092 6003168 6025099 6067664 6168138 |
Recalling Firm/
Manufacturer |
Cook Inc.
750 N Daniels Way
Bloomington IN 47404-9120
|
| For Additional Information Contact |
Cook Medical Customer Relations Departme
800-457-4500
|
Manufacturer Reason
for Recall |
A manufacturing process may lead to catheter tip fracture and or separation. Potential adverse events may include loss of device function, medical intervention to retrieve a separated segment, or complications resulting from a separated tip occluding blood flow to end organs. These catheters are used in venous or arterial pressure monitoring, blood sampling, and administration of drugs and fluids.
|
FDA Determined
Cause 2 |
Process control |
| Action |
On 1/6/2016, URGENT: MEDICAL DEVICE RECALL notifications were sent to the affected distributors and hospital Risk Management/Recall Administration via courier with instructions for identifying and returning the affected product. The recall notification included a description of the reason for the recall, affected product, consignee responsibilities, and instructions for responding to the formal recall notification. Should you have any questions or concerns, please do not hesitate to contact Cook Medical Customer Relations at (800) 457-4500 or 1(812) 339-2235. |
| Quantity in Commerce |
12691 |
| Distribution |
Worldwide Distribution - US Nationwide including DC and PR including the countries of Australia, Germany, China, Chile, Dominican Republic, Panama, Israel, Brazil, Canada |
| Total Product Life Cycle |
TPLC Device Report
|
|
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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