Haag-Streit USA Inc recalls
Every recall we track for Haag-Streit USA Inc — 7 in all, from 2019–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
7 recalls since 2017.
All FDA recall records for Haag-Streit USA Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 3 | 0 | 0 | 3 |
| 2020 | 0 | 1 | 0 | 0 | 1 |
| 2021 | 0 | 2 | 1 | 0 | 3 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Haag-Streit USA Inc recalls
What to do if you have a recalled Haag-Streit USA Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Haag-Streit USA Inc recalls
4 shown- Use cautionMedical device
Haag-Streit USA Inc recalls OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4
Haag-Streit USA recalls OCT-Camera 211 01 A3 with iOCT-Control 3 v1.4 software due to potential laser beam shut-off failure. Affected units have serial numbers 0157, 0158, or 0171.
Haag-Stre: USANov 3, 2021 - Lower riskMedical device
Haag-Streit USA Inc recalls Eyesuite 9.3.1 software, LENSTAR, MODEL LS900: ac-powered slit-lamp biomicroscope.
Haag-Streit recalls Eyesuite 9.3.1 software for LENSTAR LS900 slit-lamp biomicroscopes due to potential mixing of patient data and names when printing PDFs at Pacific Coast and Laser Institute. Affected units may need software updates.
Haag-StreitApr 15, 2021 - Use cautionMedical device
Haag-Streit USA Inc recalls Haag Streit Surgical Floor stands FS 2-11 (Ref no. 615H511) and FS 2-15 (Ref no. 615H515) in combination with the
Haag-Streit recalls surgical floor stands FS 2-11 and FS 2-15 with specific software versions that may cause eye injury during use in ophthalmology. Affected units have serial numbers starting from 1001.
Haag-StreitNov 20, 2020 - Use cautionMedical device
Haag-Streit USA Inc recalls HS Hi-R NEO 900A NIR Reference # 657 822 Serial # from 101 Product Usage: A wide range of surgical interventions are
Haag-Streit recalls specific models of surgical microscopes with software errors that may cause incorrect surgical measurements during procedures. Affected units include certain FS 2-21, FS 2-25, and FS 3-45 floor stands with specific serial numbers and software versions.
Haag-StreitJul 31, 2019
Haag-Streit USA Inc recall questions
How many recalls has Haag-Streit USA Inc had?
7 recalls from Haag-Streit USA Inc are on record with U.S. safety agencies, from 2019–2021.
What is the most recent Haag-Streit USA Inc recall?
Haag-Streit USA Inc recalls OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4, dated Nov 3, 2021. Every Haag-Streit USA Inc recall is listed on this page, newest first.
Why are Haag-Streit USA Inc products recalled?
The most common reasons on record: software error in the central control unit of the floor stand. (3).
What should I do if I have a recalled Haag-Streit USA Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Haag-Streit USA Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.