U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
Certain lots of in vitro fertilization (ivf) products were distributed without completed finished device quality testing with potential adverse events that may include nonviable gametes and/or nonviable embryos.
조치
Cook Medical sent an Urgent Medical Device Recall dated December 19, 2017 to customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to:
1. Examine inventory immediately and quarantine affected product(s).
2. Return products to Cook with the Acknowledgement and Receipt Form to receive a product credit.
3. Complete and return the Acknowledgement and Receipt Form within 5 business days of receiving this letter.
4.Report adverse events to Cook.
For questions contact Cook Medical Customer Relations at 800-457-4500 or 812-339-2235.
Worldwide Distribution - U.S. Nationwide in the states of: CA, CO, FL, IN, MA, NE, NJ, OH, TN, TX, and WI. and countries of Belarus, Belgium, Brazil, Canada, Chile, China, Egypt, Italy, Japan, Poland, Saudi Arabia, Spain, and United Kingdom.
제품 설명
Norm-Ject Tuberkulin Syringe, Catalog Number: K-ATS-1000, Global Product Number: G19871 || Product Usage: || Used to place in vitro fertilized (IVF) embryos into the uterine cavity. Intended for one-time use