PlainRecalls

Universal Meditech Inc.

Compiled from official public sources by the publisher.

28 recalls on record · Latest: Nov 1, 2023

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Agency notice ledger

Federal filing book Universal Meditech Inc. MID-BOOK · SINGLE-AGENCY

#592 of 14,151 · 28 notices · 0.027% archive

  • BOOK 28 notices
  • RANK #592 of 14,151
  • SHARE 0.027% archive
  • AGENCY FDA Devices (28)
  • CAT medical devices
  • CATS 1 category
  • LATEST Nov 1, 2023
  • PHOTO Apollo Care, LLC

Nearest notice-volume peer: Apollo Care, LLC (0 notice gap)

Universal Meditech Inc. accounts for about 0.027% of the 104,423-notice archive on 28 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Universal Meditech Inc. compares to 14,151 recalling firms

Universal Meditech Inc. ranks 592nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Universal Meditech Inc. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

28 592nd of 14151 higher than 13,557 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Universal Meditech Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Universal Meditech Inc. holds about 0.027% of archive notices alongside 28 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 1, 2023

DiagnosUS SARS-CoV-2 Antibody (IgG/IgM) Test REF 555-10
FDA Devices Moderate Nov 1, 2023

PrestiBio Rapid Detection Pregnancy Test Midstream REF 100-17 3 TESTS
FDA Devices Moderate Nov 1, 2023

PrestiBio URINALASYS TEST STRIP 10 PARAMETERS REF 900-10
FDA Devices Moderate Nov 1, 2023

DiagnosUS Pregnancy Test Midstream REF 100-17
FDA Devices Moderate Nov 1, 2023

PrestiBio KETONE TEST STRIPS REF 900-1KET 100 STRIPS/+50 FREE
FDA Devices Moderate Nov 1, 2023

Lem Fertility hCG Pregnancy Urine Test REF 100-12
FDA Devices Moderate Nov 1, 2023

DeTec hCG Pregnancy Urine Test Cassette Format, REG Cat: 100-13
FDA Devices Moderate Nov 1, 2023

OMTMO One Step Ovulation (LH) Test Strips REF 200-07
FDA Devices Moderate Nov 1, 2023

One Step Pregnancy Test REF 100-01
FDA Devices Moderate Nov 1, 2023

HealthyWiser UriTest" 10 Parameter Reagent Test Strips for Urinalysis REF 900-10
FDA Devices Moderate Nov 1, 2023

PrestiBio Ovulation Strips REF 200-4 60 LH Test Strips
FDA Devices Moderate Nov 1, 2023

DiagnosUS¿ One Step FSH Menopausal Test (Strip) REF 210-07
FDA Devices Moderate Nov 1, 2023

PrestiBio Ovulation and Pregnancy Strips REF 100-4 and REF 200-4 60 LH Test Strips/+30 HCF Test Strips
FDA Devices Moderate Nov 1, 2023

DiagnosUS hCG Pregnancy Urine Test Cassette Format REF 100-13
FDA Devices Moderate Nov 1, 2023

DiagnosUS One Step LH Ovulation Test Strip REF 200-07
FDA Devices Moderate Nov 1, 2023

DiagnosUS hCG Pregnancy Serum/Urine Test Cassette Format REF 100-27
FDA Devices Moderate Nov 1, 2023

HealthyWiser UriTest" UTI Test Strips REF 900-UTI
FDA Devices Moderate Nov 1, 2023

DiagnosUS hCG Pregnancy Urine Test Strip Format REF 100-12
FDA Devices Moderate Nov 1, 2023

HealthyWiser pH-Aware pH 4.5 - 9.0 pH Test Strips REF 900-1P 120 STRIP
FDA Devices Moderate Nov 1, 2023

DiagnosUS Ovulation Predictor Midstream REF 200-17
FDA Devices Moderate Nov 1, 2023

Lem Fertility LH Ovulation Test (Strip) REF 200-07
FDA Devices Moderate Nov 1, 2023

One Step Ovulation Test REF 200-01
FDA Devices Moderate Nov 1, 2023

HealthyWiser KetoFast" Ketone Test Strips REF 900-1K 150 test strips
FDA Devices Moderate Nov 1, 2023

To Life hCG Pregnancy Urine Test Strips Format REF Cat No: 100-10
FDA Devices Moderate Nov 1, 2023

PrestiBio BREAST MILK ALCOHOL TEST STRIP REF 910-10 25 TESTS
FDA Devices Moderate Nov 1, 2023

Am I Pregnant? One Step HCG Pregnancy Test REF 100-17
FDA Devices Moderate Nov 1, 2023

PrestiBio Pregnancy Strips REF 100-4 25 HCG Test Strips
FDA Devices Critical Feb 8, 2023

Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1 KIT Green and white box under the brand DiagnosUS, and, White box without brand name labeled as "SARS -COV-2 ANTIGEN DEVELOPMENT MADE IN USA ORAL SWAB TESTING

Universal Meditech Inc. holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Arthrex, Inc. 28 Coloplast Manufacturing US, LLC 28 Ecolab Inc 28 Zimmer Surgical Inc 28

Frequently Asked Questions

How many federal recall notices name Universal Meditech Inc.? ▼
PlainRecalls indexes 28 distinct federal recall events naming Universal Meditech Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Universal Meditech Inc. sit among other recalling firms? ▼
Universal Meditech Inc. ranks #592 of 14,151 by distinct recall-event count among 14,151 firms in this archive (96th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Universal Meditech Inc.'s notices? ▼
FDA Devices accounts for 28 of this firm's 28 indexed notices.
What product category dominates Universal Meditech Inc.'s filing book? ▼
Filings for Universal Meditech Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Universal Meditech Inc.: 28 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Universal Meditech Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026