Device brand name · Intraocular lens
Collamer Foldable Posterior Chamber Lens: medical device reports filed with FDA
174 reports name it, 2002–2004. Manufacturer given most often on reports: Staar Surgical. Product code HQL.
- 174
- device reports naming the brand
- 0% of all MAUDE reports · about 7 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 49.4%
- classified as malfunction
- 52.8% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
174 medical device reports received by FDA name the brand "Collamer Foldable Posterior Chamber Lens" (intraocular lens); the manufacturer given most often on reports is Staar Surgical; received from March 2002 to September 2004. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
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 injury (50%), malfunction (49.4%) and other (0.6%); across all intraocular lens reports (product code HQL) death is recorded in 0% and malfunction in 52.8%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are explanted (46%), device damaged prior to use (27.6%) and tears, rips, holes in device, device material (24.7%). The patient problems coded most often are surgical procedure, visual impairment and other (for use when an appropriate patient code cannot be identified). 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."
Reports by month, five years
No report naming Collamer Foldable Posterior Chamber Lens was received in the five years to August 2026; the latest was received in September 2004.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 79,755 reports carrying product code HQL. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Explanted | 80 | 46% | 7.3% |
| Device damaged prior to usethe device was damaged before use | 48 | 27.6% | 1.2% |
| Tears, rips, holes in device, device material | 43 | 24.7% | 2.1% |
| Device remains implanted | 27 | 15.5% | 4.3% |
| Other (for use when an appropriate device code cannot be identified) | 18 | 10.3% | 2.2% |
| Lens (iol), torn, split, cracked | 16 | 9.2% | 4.7% |
| Device, removal of (non-implant) | 12 | 6.9% | 1% |
| Lens replacement | 11 | 6.3% | 4.1% |
| Replace | 8 | 4.6% | 1.7% |
| Difficult to insertthe device was hard to insert | 6 | 3.4% | 1.5% |
| Lens (iol), defective, problem not specified | 6 | 3.4% | 0.1% |
| Breakthe device broke | 4 | 2.3% | 9.8% |
| Defective devicethe device was defective | 4 | 2.3% | 1.9% |
| Lens (iol), dislocated intraocular | 4 | 2.3% | 0.4% |
| Difficult to removethe device was hard to remove | 2 | 1.1% | 0.2% |
| Haptic(s), broken | 2 | 1.1% | 2.7% |
| Improper or incorrect procedure or method | 2 | 1.1% | 0.3% |
| Method, improper/incorrect | 2 | 1.1% | 0% |
| Crackthe device cracked | 1 | 0.6% | 2.8% |
| Dent in material | 1 | 0.6% | 0.1% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Surgical procedure | 92 | 52.9% |
| Visual impairmentreduced vision | 36 | 20.7% |
| Other (for use when an appropriate patient code cannot be identified) | 34 | 19.5% |
| Membrane, breakage of | 32 | 18.4% |
| Vitrectomy | 25 | 14.4% |
| Surgical procedure, additional | 19 | 10.9% |
| Capsular bag tear | 17 | 9.8% |
| Endophthalmitisinfection inside the eye | 10 | 5.7% |
| Treatment with medication(s) | 10 | 5.7% |
| Lens, replacement of | 7 | 4% |
| Surgical incision, enlargement of | 6 | 3.4% |
| Surgical procedure, repeated | 4 | 2.3% |
| Therapy/non-surgical treatment, additional | 4 | 2.3% |
| Hypopyon | 2 | 1.1% |
| Surgical procedure aborted/stopped | 2 | 1.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Collamer Foldable Posterior Chamber Lens | Product code HQL | All MAUDE reports |
|---|---|---|---|
| Reports | 174 | 79,755 | 26,136,888 |
| Share of that pool | — | 0.2% | 0% |
| Classified as death, per 1,000 reports | 0 | 0 | 9 |
| Classified as injury | 50% | 42.8% | 36.2% |
| Classified as malfunction | 49.4% | 52.8% | 62.3% |
| Filed by the manufacturer | 100% | 98.2% | 94.9% |
Shares are of reports, not 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."
Other brands with product code HQL
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Acrysof | 9,161 | 0 | 0% |
| Tecnis Simplicity | 5,310 | 1,217 | 0% |
| Tecnis Iol | 5,901 | 715 | 0% |
| Tecnis | 3,082 | 0 | 0.1% |
| Tecnis Itec Preloaded 1-Piece Iol | 2,435 | 0 | 0% |
| AcrySof IQ Natural Singlepiece IOL | 2,424 | 118 | 0% |
| Clareon IOL with the AutonoME Delivery System | 2,276 | 864 | 0% |
| Tecnis 1-Piece | 2,259 | 0 | 0% |
| enVista Intraocular Lens | 2,163 | 36 | 0% |
| Hydroview Intraocular Lens | 2,067 | 0 | 0% |
| Acrysof Restor | 3,801 | 0 | 0% |
| Acrysof Iq Toric | 1,905 | 0 | 0% |
| AcrySof Multipiece IOL | 1,619 | 298 | 0% |
| Silicone Advanced Optic-Violet Shield | 1,413 | 0 | 0% |
| AcrySof Singlepiece IOL | 1,211 | 131 | 0% |
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." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Collamer Foldable Posterior Chamber Lens reports
How many FDA reports name Collamer Foldable Posterior Chamber Lens?
174 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
injury (50%), malfunction (49.4%) and other (0.6%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
explanted (46%), device damaged prior to use (27.6%), tears, rips, holes in device, device material (24.7%), device remains implanted (15.5%) and other (for use when an appropriate device code cannot be identified) (10.3%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Collamer Foldable Posterior Chamber Lens was at fault?
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." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
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. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. 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.