Device manufacturer, as written on reports

Lifescan Europe A Division Of Cilag Intl: medical device reports filed with FDA

223,383 reports name it as the manufacturer of the device involved, 2011–2019.

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.

223,383
reports naming it as manufacturer: 0.9% of all MAUDE reports; 0
reports, 12 months to August 2026: 0 in the 12 months before; 95.5%
classified as malfunction: 62.3% across all reports; 0%
classified as death, as reported: 0.9% across all reports

223,383 medical device reports received by FDA give Lifescan Europe A Division Of Cilag Intl as the manufacturer of the device involved, 0.9% of the MAUDE database, from May 2011 to April 2019. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

0 reports arrived in the 12 months to August 2026, and none 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 (95.5%) and injury (4.2%). 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	Classified as death
Ot Verio Iq Meter	System, test, blood glucose, over the counter	92,505	0%
Ot Verio2 Meter	System, test, blood glucose, over the counter	44,750	0%
Ot Ping Meter	System, test, blood glucose, over the counter	25,129	0%
Ot Ultralink Meter	System, test, blood glucose, over the counter	13,622	0%
Ot Verio Flex Meter	System, test, blood glucose, over the counter	12,351	0%
Ot Verio Pro Meter	System, test, blood glucose, over the counter	6,701	0%
Ot Verio Test Strips	System, test, blood glucose, over the counter	6,325	0%
Ot Ping Enhanced Meter	System, test, blood glucose, over the counter	4,763	0%
Ot Veriovue Meter	System, test, blood glucose, over the counter	3,986	0%
Ot Ultra2 Meter	System, test, blood glucose, over the counter	2,699	0%
Ot Verio Meter	System, test, blood glucose, over the counter	2,683	0%
Ot Verio Sync Meter	System, test, blood glucose, over the counter	2,273	0%
Ot Ultramini Meter	System, test, blood glucose, over the counter	1,747	0.1%
Ot Verio Pro Plus Meter	System, test, blood glucose, over the counter	1,529	0%
Ot Ultra Meter	System, test, blood glucose, over the counter	567	0.1%
Ot Ultrasmart Meter	System, test, blood glucose, over the counter	259	0%
Ot Select Simple Meter	System, test, blood glucose, over the counter	124	0%
Ot Delica Lancing Device	System, test, blood glucose, over the counter	121	0%
Ot Ultra Easy Meter	System, test, blood glucose, over the counter	111	0.6%
Ot Vita Meter	System, test, blood glucose, over the counter	85	0%
Ot Select Meter	System, test, blood glucose, over the counter	73	0%
Unknown Meter	System, test, blood glucose, over the counter	71	0%
One Touch Lancing Device	System, test, blood glucose, over the counter	62	0%
Ot Basic Enhanced Meter	System, test, blood glucose, over the counter	4	0%

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	223,309	100%
LZG	Pump, infusion, insulin	35	0%
CGA	Glucose oxidase, glucose	27	0%
FMK	Single use only blood lancet with an integral sharps injury prevention feature	8	0%
LFR	Glucose dehydrogenase, glucose	3	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

Death0%4

Injury4.2%9,366

Malfunction95.5%213,314

Other0%2

Not given0.3%697

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

Questions about Lifescan Europe A Division Of Cilag Intl reports

How many FDA device reports name Lifescan Europe A Division Of Cilag Intl as manufacturer?

223,383 reports through August 2026, 0 of them in the latest 12 months.

Which of its brands appear most often?

Ot Verio Iq Meter (92,505), Ot Verio2 Meter (44,750), Ot Ping Meter (25,129), Ot Ultralink Meter (13,622) and Ot Verio Flex Meter (12,351).

Which device types does it report on?

system, test, blood glucose, over the counter (100%), pump, infusion, insulin (0%), glucose oxidase, glucose (0%) and single use only blood lancet with an integral sharps injury prevention feature (0%).

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.