CLASS II Device recall · Reported 12 Aug 2020 · FDA Enforcement Report

Siemens Healthineers Uroskop Omnia max recalled

Siemens Medical Solutions USA is recalling Siemens Healthineers Uroskop Omnia max, distributed nationwide in the US. The recall was initiated on 8 Jan 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSerial Numbers: 4557 4574 4571 4099 4074 4014 4627 4626 4578 4645 4316 4615 4056 4587 4049 4068 4305 4015 4543 4616 4553 4333 4063 4655 4556 4022 4521 4121 4325 4111 4510 4565 4322 4554 4301 4597 4509 4661 4036 4519 4520 4043 4024 4560 4629 4530 4646 4318 4618 4575 4304 4142 4300 4095 4146 4649 4059 4562 4501 4309 4548 4313 4119 4135 4069 4020 4032 4612 4512 4053 4663 4061 4590 4593 4642 4312 4528 4060 4051 4506 4025 4037 4635 4054 4042 4033 4544 4541 4566 4132 4067 4120 4613 4112 4335 4336 4072 4652 4055 4108 4559 4511 4540 4126 4129 4104 4307 4334 4073 4631 4582 4570 4561 4641 4052 4572 4047 4134 4605 4326 4529 4603 4568 4654 4532 4102 4130 4317 4505 4062 4594 4096 4585 4637 4085 4143 4516 4662 4086 4598 4118 4573 4101 4589 4100 4321 4558 4591 4105 4106 4513 4538 4098 4537 4306 4539 4066 4310 4651 4624 4314 4545 4552 4082 4664 4125 4328 4124 4636 4329 4600 4601 4602 4094 4114 4117 4136 4303 4319 4140 4141 4500 4531 4630 4622 4535 4580 4660 4330 4332 4133 4588 4609

Quantity recalled194 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2757-2020
FDA event ID: 85999
Recalling firm: Siemens Medical Solutions USA, Malvern, PA
Classification: Class II
Status: Terminated
Recall initiated: 8 Jan 2020
FDA classified: 5 Aug 2020
Reported: 12 Aug 2020
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Device Malfunction
Device type: Imaging Equipment

Timeline

8 Jan 2020	Recall initiated by company
5 Aug 2020	Classified by FDA	+210 days
12 Aug 2020	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Two software issues (1) Using the override function in case of blocked system movements affecting Luminos dRF Max, Luminos Agile Max and Uroskop Omnia Max systems may cause collision of the system under operator control with obstacles or persons .(2) Incorrectly assigned image affecting Ysio Max, Luminos dRF Max and Luminos Agile Max systems with detector MAX Static causing incorrect base for diagnosis

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.

Where it was distributed

US Nationwide distribution.

Nationwide

Questions about this recall

Why was it recalled?

Which lots are affected?

Serial Numbers: 4557 4574 4571 4099 4074 4014 4627 4626 4578 4645 4316 4615 4056 4587 4049 4068 4305 4015 4543 4616 4553 4333 4063 4655 4556 4022 4521 4121 4325 4111 4510 4565 4322 4554 4301 4597 4509 4661 4036 4519 4520 4043 4024 4560 4629 4530 4646 4318 4618 4575 4304 4142 4300 4095 4146 4649 4059 4562 4501 4309 4548 4313 4119 4135 4069 4020 4032 4612 4512 4053 4663 4061 4590 4593 4642 4312 4528 4060 4051 4506 4025 4037 4635 4054 4042 4033 4544 4541 4566 4132 4067 4120 4613 4112 4335 4336 4072 4652 4055 4108 4559 4511 4540 4126 4129 4104 4307 4334 4073 4631 4582 4570 4561 4641 4052 4572 4047 4134 4605 4326 4529 4603 4568 4654 4532 4102 4130 4317 4505 4062 4594 4096 4585 4637 4085 4143 4516 4662 4086 4598 4118 4573 4101 4589 4100 4321 4558 4591 4105 4106 4513 4538 4098 4537 4306 4539 4066 4310 4651 4624 4314 4545 4552 4082 4664 4125 4328 4124 4636 4329 4600 4601 4602 4094 4114 4117 4136 4303 4319 4140 4141 4500 4531 4630 4622 4535 4580 4660 4330 4332 4133 4588 4609

Where was it sold?

US Nationwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 85999

Reported	Class	Recall	Company	Reason	Where
12 Aug 2020	CLASS II	Siemens Healthineers Ysio Max recalled by Siemens Medical Solutions USA	Siemens Medical Solutions USA	Device Malfunction	Nationwide
12 Aug 2020	CLASS II	Siemens Healthineers Luminos Agile Max recalled	Siemens Medical Solutions USA	Device Malfunction	Nationwide
12 Aug 2020	CLASS II	Siemens Healthineers Luminos dRF Max recalled	Siemens Medical Solutions USA	Device Malfunction	Nationwide

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