• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Enforcement Report - Week of April 2, 2014

  • Print
  • Share
  • E-mail
-

Product Detail

Product Description AMS AST For the In vitro quantitative determination of AST in serum Quantitative determination of AST in serum.
Recall Number Z-1269-2014
Classification Class II
Code Info Model Numbers: 40072, 40146, 80146. Lot codes: 131083, 131084, 131085, 131086, 131087, 131088, 131089, 1310810, 1310811, 1310812, 1310813, 1310814, 1310815, 141081.
Product Distributed Qty 116 kits
Reason For Recall Marketing the devices outside 510(k) requirements

Event Detail

Event Id 67599
Product Type Devices
Status Ongoing
Recalling Firm AMS Diagnostics, LLC
City Weston
State FL
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2014-02-11
Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Distribution Pattern Nationwide Distribution including FL, GA, MD, CA, NC, MA, SC, WY, and TX.
-
-