Liebel-Flarsheim Company recalls

Liebel-Flarsheim Company has 4 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 19 Aug 2026. 1 is still ongoing. 1 was reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls4since 2018

Last 12 months1reported

Class I125% of total

Ongoing1latest 19 Aug 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 1 0

Severity split

Class I 1 25%Class II 3 75%Class III 0 0%

Why liebel-flarsheim company is recalled

Device Malfunction375%
Particulate Matter125%

Product types

Imaging Equipment375%
Injectable & IV Drugs125%

By year

2026125%
2021125%
2018250%

Ongoing liebel-flarsheim company recalls

1 active

Reported	Class	Recall	Company	Reason	Where
19 Aug 2026Drug	CLASS I	Optiray Imaging -350, Ioversol Injection recalledOptiray	Liebel-Flarsheim Company	Particulate Matter	Nationwide

All liebel-flarsheim company recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
19 Aug 2026Drug	CLASS I	Optiray Imaging -350, Ioversol Injection recalledOptiray	Liebel-Flarsheim Company	Particulate Matter	Nationwide
14 Jul 2021Device	CLASS II	HydraVision Digital Imaging System Product ID recalled	Liebel-flarsheim Company	Device Malfunction	Nationwide
29 Aug 2018Device	CLASS II	Hydra Vision Urology X-Ray System recalled by Liebel-flarsheim Company	Liebel-flarsheim Company	Device Malfunction	30 states
29 Aug 2018Device	CLASS II	Direct Digital Imaging System recalled by Liebel-flarsheim Company	Liebel-flarsheim Company	Device Malfunction	30 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.