Visual, pregnancy hcg, prescription use: medical device reports filed with FDA

3,859 reports carry this product code, 1996–2026; 11 brands with a page.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

3,859
reports with this product code: 0% of all MAUDE reports; 218
reports, 12 months to August 2026: 292 in the 12 months before; 86.3%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

Product code JHI is FDA's classification for "Visual, pregnancy hcg, prescription use" (clinical Chemistry panel), a class 2 device. 3,859 medical device reports carry this product code, 0% of the MAUDE database, from July 1996 to August 2026.

218 reports arrived in the 12 months to August 2026, down 25% from 292 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (86.3%), other (8.2%) and injury (5.1%). 11 brand names with a page on this site carry this code; the brands table is ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction
Axsym Total Bhcg	268	0	0%	68.8%
Consult Hcg Urine Cassette 5001 25t	152	0	0%	94.1%
Clinitek Status+	48	25	0%	83.7%
Architect I2000sr Analyzer	25	0	0.1%	95.2%
Abbott Axsym System	14	0	0%	54.4%
Dimension	10	40	0.1%	98.5%
Synchron Lx I 725 Clinical System	5	0	0%	73.1%
Access Immunoassay System	2	0	0%	31%
Architect I2000 Analyzer	2	0	0%	91.5%
Cobas 6000 E 601 Module	2	0	0%	99.7%
Vitros Eci Immunodiagnostic System	1	0	0%	99.6%

Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Manufacturers named

Manufacturer (as written on reports)	Reports	Share
Alere San Diego	2,373	61.5%
Beckman Coulter	202	5.2%
Biosite	159	4.1%
Siemens Healthcare Diagnostics	159	4.1%
Abbott Manufacturing	60	1.6%
Biomerieux	10	0.3%
Dade Behring	10	0.3%
Abbott Laboratories	8	0.2%
Ortho-Clinical Diagnostics	8	0.2%
Quidel	4	0.1%
Tosoh	1	0%

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type and report source

Event type

Death0%1

Injury5.1%197

Malfunction86.3%3,331

Other8.2%315

Not given0.4%15

Who filed

Manufacturer report98%3,780

Voluntary report1.1%42

User facility report0%0

Distributor report0.4%16

Not given0.5%21

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
False negative result	1,668	43.2%
False positive result	1,384	35.9%
Incorrect, inadequate or imprecise result or readings	379	9.8%
Incorrect or inadequate test results	246	6.4%
High test results	83	2.2%
Low test results	57	1.5%
Device displays incorrect message	39	1%
Insufficient device problem information	12	0.3%
Contamination	11	0.3%
Improper or incorrect procedure or method	10	0.3%
False reading from device non-compliance	8	0.2%
Method, improper/incorrect	8	0.2%
Non reproducible results	6	0.2%
Unable to obtain readings	6	0.2%
High readingsreadings were too high	5	0.1%
Low readingsreadings were too low	5	0.1%
Product quality problem	4	0.1%
Replace	4	0.1%
Calibration error	3	0.1%
Device issuea problem with the device	3	0.1%

Questions about visual, pregnancy hcg, prescription use reports

What is product code JHI?

FDA's classification code for "Visual, pregnancy hcg, prescription use", class 2, reviewed by the clinical Chemistry panel. Every device report carries the product code of the device involved.

How many reports carry this code?

3,859 reports through August 2026, 218 of them in the latest 12 months.

Which brands appear most often?

Axsym Total Bhcg (268), Consult Hcg Urine Cassette 5001 25t (152), Clinitek Status+ (48), Architect I2000sr Analyzer (25) and Abbott Axsym System (14). Widely used products collect more reports because more people use them.

Can the brands table be used to rank the devices?

No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." Brands differ in how many are in use, how long they have been sold and how reports are collected.

Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.