Uroskop Omnia Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic…
Medical device recall Z-1168-2023. Published in FDA’s Enforcement Report on Mar 1, 2023.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Mar 1, 2023. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 7 units; Exanded recall: 215 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Potential risk of collision with the ceiling, wall, or objects which may result in serious injury to staff or patients due to room configuration parameters of the system being set to default values
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Uroskop Omnia Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762473
7 units; Exanded recall: 215 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
UDI: 4056869008981 S/N: 4645 4556 4510 5144 4307 4594 4125 Expanded Recall 2/24/23: 4014 4015 4020 4022 4032 4033 4042 4047 4055 4059 4061 4062 4063 4067 4068 4086 4094 4096 4099 4102 4105 4106 4108 4111 4112 4114 4117 4119 4120 4126 4128…
Every code shown here, 1,158 characters
UDI: 4056869008981 S/N: 4645 4556 4510 5144 4307 4594 4125 Expanded Recall 2/24/23: 4014 4015 4020 4022 4032 4033 4042 4047 4055 4059 4061 4062 4063 4067 4068 4086 4094 4096 4099 4102 4105 4106 4108 4111 4112 4114 4117 4119 4120 4126 4128 4129 4130 4132 4134 4135 4136 4141 4142 4146 4303 4305 4306 4310 4312 4314 4316 4318 4319 4325 4326 4329 4330 4332 4500 4501 4509 4513 4516 4519 4520 4529 4531 4532 4535 4537 4538 4540 4541 4543 4544 4548 4552 4553 4554 4557 4559 4561 4562 4565 4566 4570 4575 4580 4582 4585 4587 4588 4591 4593 4597 4600 4601 4602 4603 4605 4609 4616 4626 4627 4629 4630 4631 4635 4636 4637 4641 4651 4659 4660 5026 5028 5030 5031 5033 5049 5051 5061 5062 5064 5066 5069 5072 5074 5078 5084 5088 5093 5101 5103 5107 5108 5112 5114 5116 5118 5123 5124 5128 5130 5133 5134 5135 5137 5139 5140 5142 5146 5152 5159 5163 5173 5174 5175 5186 5187 5190 5191 5196 5197 5198 5199 5208 5215 5221 5222 5232 5240 5258 5267 5268 5278 6013 6021 6023 6034 6035 6038 6039 6043 6044 6048 6050 6054 6062 6064 6065 6066 6069 6072 6078 6079 6080 6085 6090 6091 6096 6113 6120 6121 6127 6129 6131 6134 6136 6141 6146 6149 6154 6157 6163 6165 6168 6169 6176
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
US Nationwide distribution.
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Dec 21, 2022.
- FDA classified it on Feb 23, 2023.
- FDA’s Enforcement Report published it on Mar 1, 2023.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Siemens Medical Solutions USA, Inc, of Malvern, PA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: N/A.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.