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Tex-Care Medical

Flynt/Amtex, Inc. · Model 91301-350 · UDI-DI 00632195001908

ITG
10
510(k) clearances
111
Adverse events
3
Recalls
241
Facilities

Description

3"X50YD BIAS CC UNBOXED

Recalls

DateFirmReason
2026-01-15KOB GmbHDue to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
2017-08-18Integra LifeSciences Corp.A quarantined lot of the devices was released for sale. Devices from this lot may experience increased exothermic reaction causing higher levels of heat output which exceed the pro
2013-08-053M Company - Health Care Business3M is conducting a voluntary product recall of selected lots of 3M" Scotchcast" Wet or Dry Cast Padding. Upon investigation of a health care provider feedback, and confirmed with

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.