RegWardenFDA facility compliance records
Company

PRINCETON BIOMEDITECH CORP.

2 recall(s) on record — most severe on record: Class II.

Recalls by year

FDA actions on record by year2012: 1 recalls; 2024: 1 recalls1’12’13’14’15’16’17’18’19’20’21’22’231’24’25’26
  • Recalls (2)

Registered facilities (3)

Recalls & enforcement

  • Class IIOngoing2024-08-23
    This recall was initiated due to customer complaints of false negative of hCG test results when running patient urine samples. Use of the above listed product lot may result in false negative results. An end user reported that the OSOM Ultra hCG Combo Test, lot 563L13, produced f…
  • Class IITerminated2012-03-09
    There have been reports of dual positive (Flu A + Flu B positive) results being encountered.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “PRINCETON BIOMEDITECH CORP. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-2246703-princeton-biomeditech-corp/

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