FDA Media Alert Detail

Device Recall

FDA Device Recall: healthmark ProChek-II, Model Number PT-313, PT-201-12

  • U.S. Food and Drug Administration
  • September 2, 2026
  • ID: device-Z-3031-2026

Device Enforcement Report Details

Recall NumberZ-3031-2026
Recalling FirmHealthmark Industries Co., Inc.
ClassificationClass II
Voluntary / MandatedVoluntary: Firm initiated
Distribution PatternWorldwide distribution - US Nationwide and the countries of Canada, France, Hong Kong, South Korea.
StatusOngoing
Device ClassN/A
Device NameN/A
Product Description

healthmark ProChek-II, Model Number PT-313, PT-201-12

Reason for Recall

Test manufactured with an expired ingredient which may present as either a false negative or positive.

Code Information

PT-313 - Serial/Lot Numbers: 3000535312, 3000535333, 3000536416, 3000536423, 3000537810, 3000537822, 3000542453, 3000545623, 3000550099, 3000550512, 313069, 313072, 313073, 313074, 313075, 313076, 313077, 313078, 313079, 313080, 313081, 313082, 313083, 313084, 313085, 313086, 313087, 313088, 313089, 313090, 313091, 313092, 313093, 313094, 313095, 313096, 313097, 313098, 313099, 313100, 313101, 313102, 313106, 313107; H-PT-201-12 - Serial/Lot Numbers: 7P0110, 7P0111, 7P0113, 7P0122.


Content syndicated from the U.S. Food and Drug Administration (FDA) device enforcement reports database.