Z-1621-2016 Class II Terminated
FDA device recall Z-1621-2016 was initiated by Applied Medical Resources Corp on April 1, 2016 and is designated Class II. Reason for recall: Increased customer complaints indicating inconsistent clip application; may lead to unoccluded vessels. The recall status is terminated (terminated February 7, 2017). Affected quantity: 559,274.
Recall Details
- Product Type
- Devices
- Report Date
- May 18, 2016
- Initiation Date
- April 1, 2016
- Termination Date
- February 7, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 559,274
Product Description
Reason for Recall
Distribution Pattern
U.S. distribution to the following: IL, IN, WY, PA, CA, LA, MN, AZ, OH, OR, CT, WI, NC, AK, NE, MI, KS, FL, MN, TN, SC, MA, MD, KY, TX, GA, TX, NJ, MO, CO, MS, MT, ID, ME, VA, NY, UT, MI, AL, PR, NM, DE, OK, WA, DC, NH, AR Foreign distribution to the following; Australia, Spain, New Zealand, Italy, Israel, Estonia, United Arab Emirates, Germany, Netherlands, France, Kuwait, Korea, Qatar, Mexico, Switzerland, Austria, Bahrain, Lebanon, Brazil, Belgium, United Kingdom, Finland, Japan, Argentina, Ireland, Iran, Denmark, Norway, Colombia, Serbia, Uruguay, Sweden, Canada, Costa Rica, South Africa, Czech Republic, Chile, Finland, India, Thailand, Malaysia