LIEBEL-FLARSHEIM COMPANY LLC recalls
Every recall we track for LIEBEL-FLARSHEIM COMPANY LLC — 2 in all, from 2021–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for LIEBEL-FLARSHEIM COMPANY LLC 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 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 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 | 1 | 0 | 1 |
What to do if you have a recalled LIEBEL-FLARSHEIM COMPANY LLC 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 LIEBEL-FLARSHEIM COMPANY LLC recalls
2 shown- Lower riskDrug
Liebel-Flarsheim Company LLC recalls Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose
Liebel-Flarsheim recalls Optiray Imaging Bulk Package-350 (Ioversol 74%) due to potential particulate matter in the injection solution. This could cause blockages or reactions if injected. Affected units have NDC 0019-1333-65 and lot # 25ZF3670.
Liebel-FlarsheimJul 31, 2026 - Lower riskMedical device
LIEBEL-FLARSHEIM COMPANY LLC recalls HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)
LIEBEL-FLARSHEIM recalls HydraVision Digital Imaging Systems with Product ID 705559 (65KW) and 705560 (80KW) due to potential overestimation of radiation dose. This may lead to unnecessary radiation exposure during medical procedures.
LIEBEL-FLARSHEIMMar 11, 2021
LIEBEL-FLARSHEIM COMPANY LLC recall questions
How many recalls has LIEBEL-FLARSHEIM COMPANY LLC had?
2 recalls from LIEBEL-FLARSHEIM COMPANY LLC are on record with U.S. safety agencies, from 2021–2026 (1 medical device, 1 drug).
What is the most recent LIEBEL-FLARSHEIM COMPANY LLC recall?
Liebel-Flarsheim Company LLC recalls Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose, dated Jul 31, 2026. Every LIEBEL-FLARSHEIM COMPANY LLC recall is listed on this page, newest first.
What should I do if I have a recalled LIEBEL-FLARSHEIM COMPANY LLC 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 LIEBEL-FLARSHEIM COMPANY LLC 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.