Device manufacturer, as written on reports

Bayer Healthcare: medical device reports filed with FDA

11,031 reports name it as the manufacturer of the device involved, 2003–2026.

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.

11,031
reports naming it as manufacturer: 0% of all MAUDE reports; 15
reports, 12 months to August 2026: 20 in the 12 months before; 76.6%
classified as malfunction: 62.3% across all reports; 0.1%
classified as death, as reported: 0.9% across all reports

11,031 medical device reports received by FDA give Bayer Healthcare as the manufacturer of the device involved, 0% of the MAUDE database, from February 2003 to July 2026. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

15 reports arrived in the 12 months to August 2026, down 25% from 20 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 (76.6%), injury (22.9%) and other (0.3%). Manufacturers are required to report events they learn of, so a large manufacturer with many products in use files many reports. 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 named most often

Brand	Device type	Reports	Latest 12 months	Classified as death
Contour Test Strips 50	System, test, blood glucose, over the counter	2,016	0	0%
Contour	System, test, blood glucose, over the counter	1,563	38	0%
Essure	Transcervical contraceptive tubal occlusion device	1,373	435	0.2%
Ascensia Contour	System, test, blood glucose, over the counter	981	0	0.1%
Contour Test Strips	System, test, blood glucose, over the counter	716	0	0%
Contour Next	System, test, blood glucose, over the counter	587	33	0%
Breeze2	System, test, blood glucose, over the counter	429	0	0%
Contour Test Strips 10	System, test, blood glucose, over the counter	215	0	0%
Ascensia Breeze	Glucose oxidase, glucose	194	0	0.5%
Ascensia Elite Xl	System, test, blood glucose, over the counter	167	0	0%
Autodisc 50 Test Strips	System, test, blood glucose, over the counter	151	0	0%
Glucometer Dex	Hexokinase, glucose	145	0	0%
Contour Ts	System, test, blood glucose, over the counter	117	0	0%
Glucometer Elite 4 Date	System, test, blood glucose, over the counter	109	0	0%
Contour Next Link	System, test, blood glucose, over the counter	88	0	0%
Contour Next EZ	System, test, blood glucose, over the counter	52	6	0%
Glucometer Elite 4 Basic	System, test, blood glucose, over the counter	29	0	0.8%

Brands with a page on this site, 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."

Device types

Product code	Device type	Reports	Share
NBW	System, test, blood glucose, over the counter	8,825	80%
HHS	Transcervical contraceptive tubal occlusion device	1,413	12.8%
CFR	Hexokinase, glucose	181	1.6%
LFR	Glucose dehydrogenase, glucose	179	1.6%
CGA	Glucose oxidase, glucose	143	1.3%
FMK	Single use only blood lancet with an integral sharps injury prevention feature	80	0.7%
KNH	Laparoscopic contraceptive tubal occlusion device	68	0.6%
LCP	Assay, glycosylated hemoglobin	51	0.5%
JJX	Single (specified) analyte controls (assayed and unassayed)	48	0.4%
JJE	Analyzer, chemistry (photometric, discrete), for clinical use	9	0.1%

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

Death0.1%8

Injury22.9%2,522

Malfunction76.6%8,445

Other0.3%34

Not given0.2%22

Grey bar: all 26,136,888 MAUDE reports. Event type is the filer's classification and is not verified by FDA.

Questions about Bayer Healthcare reports

How many FDA device reports name Bayer Healthcare as manufacturer?

11,031 reports through August 2026, 15 of them in the latest 12 months.

Which of its brands appear most often?

Contour Test Strips 50 (2,016), Contour (1,563), Essure (1,373), Ascensia Contour (981) and Contour Test Strips (716).

Which device types does it report on?

system, test, blood glucose, over the counter (80%), transcervical contraceptive tubal occlusion device (12.8%), hexokinase, glucose (1.6%) and glucose dehydrogenase, glucose (1.6%).

Does a high count say something about the manufacturer?

Not by itself. Manufacturers must file a report for every event they become aware of, so report volume follows the number of devices in use. 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."

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. Manufacturer names are pooled after company suffixes (Inc., LLC, GmbH and similar) are dropped; names that read as a person rather than an organisation are never published. 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.