RegWardenFDA facility compliance records
Recall

Class II — Polymer Technology Systems, Inc.

Recalling firmPOLYMER TECHNOLOGY SYSTEMS, INC.
Registered facilityPolymer Technology Systems (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonInternal investigation demonstrated under-recovery for glucose when tested against a reference method. This could result in a low to moderate health risk.
ProductPTS PANELS, Glucose Test Strips for use with CardioChek Brand Analyzers Product Usage: used by healthcare professionals and individuals with diabetes to measure glucose in whole blood
Quantity7048 total, 3499 in USA
DistributionWorldwide Distribution - USA Nationwide including Puerto Rico and countries of: UK, CHL, ENG, BEL, ITA, TKY, BEL, LIT, LTV, EGY, SPG, HOK, SWE, MEX, UAE, COR, ISR, MAL, AUS, POR, POL, SLN and STQ.
Initiated2013-04-04
Classified2013-05-24
Terminated2014-04-16
Recall numberZ-1403-2013
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Polymer Technology Systems, Inc. (Z-1403-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65067/

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