RegWardenFDA facility compliance records
Recall

Class I — TERRIFIC CARE LLC

Recalling firmTERRIFIC CARE LLC
Registered facilityTERRIFIC CARE LLC (the firm's only registered facility)
ClassificationClass I
StatusTerminated
ReasonPotential for abnormally high INR test results with the CoaguChek XS PT Test Strips for customers who purchased products directly from Terrific Care LLC dba MedEx Supply via website/telephone/facsimile.
ProductCoaguChek XS PT Test; All Catalog/REF Numbers that do NOT end in 160 The CoaguChek XS PT test strips are part of the CoaguChek XS System. The CoaguChek XS System is intended for properly selected and suitably trained users or their caregivers on the prescription or other order of the treating doctor.
Quantity793 boxes
DistributionNationwide Distribution
Initiated2018-12-20
Classified2019-02-01
Terminated2020-12-29
Recall numberZ-0787-2019
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 I recall — TERRIFIC CARE LLC (Z-0787-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/81857/

Not open yet

Alerts for TERRIFIC CARE LLC

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.