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Recall Observatory FDA recall evidence

Device product

AMS AST For the In vitro quantitative determination of AST in serum Quantitative determination of AST in serum.

Z-1269-2014

February 11, 2014

Class II

Product summary

Firm
AMS Diagnostics, LLC
Event
Event 67599
Status
Terminated
Classification
Class II
Quantity
116 kits
Official record key
device-enforcement:Z-1269-2014

Official wording

Reason: Marketing the devices outside 510(k) requirements

Code information: Model Numbers: 40072, 40146, 80146. Lot codes: 131083, 131084, 131085, 131086, 131087, 131088, 131089, 1310810, 1310811, 1310812, 1310813, 1310814, 1310815, 141081.

Distribution pattern: Nationwide Distribution including FL, GA, MD, CA, NC, MA, SC, WY, and TX.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Marketing the devices outside 510(k) requirements