healthmark ProChek-II, Model Number PT-313, PT-201-12 recall — FDA Z-3031-2026
Test manufactured with an expired ingredient which may present as either a false negative or positive.
Overview of recall records associated with Healthmark Industries Co., Inc., including dates, categories and classifications where available.
Classification mix: Class II: 4.
Test manufactured with an expired ingredient which may present as either a false negative or positive.
Test manufactured with an expired ingredient which may present as either a false negative or positive.
During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their…
During endoscope surveillance monitoring, a user facility identified contamination from duodenoscope samples that were linked to the Pre-filled Water Syringes as part of their…
This page summarizes recall records in which the official source identifies Healthmark Industries Co., Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.