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UFSK International OSYS Gmbh Kirchhoffstr. 1 Ratisbon Germany

UFSK International OSYS Gmbh Kirchhoffstr. 1 Ratisbon Germany Recalls

All product recalls associated with UFSK International OSYS Gmbh Kirchhoffstr. 1 Ratisbon Germany.

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Recall Summary

Total Recalls

1000

Past Year

593

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1561–1580 of 10391 recalls

UFSK Treatment Chair 500 XLE (UFSK) – Drive Mechanism Wear (2023)

Service life of the electrical seat part drive of the treatment chair may be shortened unexpectedly after several years of use due to a potential wear-related reduction in the self-locking of the drive and may remain undetected. A worsened self-locking of the seat drive can lead to overriding the drive s end position when positioning the patient with the seat part in an inclined position

FDAMay 31, 2023Nationwide• UFSK International OSYS Gmbh Kirchhoffstr. 1 Ratisbon Germany

Ziprasidone Hydrochloride Capsules (Harvard Drug Group) – Label Mix-up (2023)

Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5 mg.

Class IHigh

FDAMay 31, 2023Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

1...77 787980 81...520

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VERITAS Infusion Packs (Johnson & Johnson) – Housing Weld Defect (2023)

Weld protrusion/physical gap between the housing and pack cover, may exceed design specification, due to a manufacturing issue, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the phacoemulsification and irrigation/aspiration handpieces during surgery, which could result in surgical delay and/or longer surgical time, which could result in transient corneal edema.

FDAMay 30, 2023Nationwide• Johnson & Johnson Surgical Vision, Inc.

Enterade Oncology Formula – Potential Mold Spoilage (2023)

Potential for the product to develop mold and spoil.

Class IIModerate

FDAMay 25, 2023AL, AZ, AR +44 more• ENTRINSIC HEALTH SOLUTION INC

TruSignal AllFit Sensor: a) REF TS-AF-10, 10 pcs; B) R... (GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland) – there is a potential reduction of ene... (2023)

There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

FDAMay 19, 2023Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

TruSignal Ear Sensor, REF TS-E-D; Oximeter (GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland) – there is a potential reduction of ene... (2023)

There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

FDAMay 19, 2023Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

TruSignal Integrated Ear Sensor with GE Connector REF TS-... (GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland) – there is a potential reduction of ene... (2023)

There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

FDAMay 19, 2023Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

TruSignal Sensitive Skin Sensor, REF TS-SE-3; Oximeter (GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland) – there is a potential reduction of ene... (2023)

There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

FDAMay 19, 2023Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

DigitalDiagnost C90, Model No. 712034 and 712035 (Philips North America Llc) – there is a software login in issue th... (2023)

There is a software login in issue that may prevent the user from logging in.

FDAMay 19, 2023AZ, GA, IN +6 more• Philips North America Llc

Voalte Patient Safety, Part Number 4.0, V4.0.000 to 4.0.4... (Baxter Healthcare Corporation) – baxter identified a potential risk wh... (2023)

Baxter identified a potential risk where the "safety" monitoring and "bed exit" monitoring features may enter a permanent state of alert suppression. In this state, a caregiver may not be alerted remotely when assigned patient protocols (bed exit, siderail position, brakes off, height of bed changes, head of bed angle, and/or turn reminders) are turned off.

FDAMay 19, 2023Nationwide• Baxter Healthcare Corporation

NaviCare Patient Safety V3.9.200 to 3.9.600, used with th... (Baxter Healthcare Corporation) – baxter identified a potential risk wh... (2023)

FDAMay 19, 2023Nationwide• Baxter Healthcare Corporation

TruSignal Wrap Sensor, REF TS-W-D; Oximeter (GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland) – there is a potential reduction of ene... (2023)

There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

FDAMay 19, 2023Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

TruSignal Adult/Pediatric Sensor; Oximeter, Ear: a) RE... (GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland) – there is a potential reduction of ene... (2023)

There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.

FDAMay 19, 2023Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland

QIAstat-Dx Respiratory SARS-CoV-2 Panel -US IVD qualitati... (Qiagen GmbH Qiagen Str. 1 Hilden Germany) – identified a decreased performance re... (2023)

Identified a decreased performance reliability rate, Run abortions could cause delayed diagnosis since sample testing would have to be repeated

FDAMay 19, 2023AL, CA, DE +11 more• Qiagen GmbH Qiagen Str. 1 Hilden Germany

Allen Advance Chest Support (Baxter) – Potential Cracking (2023)

Potential for the device to crack where the Chest Base Prone support attaches to the carbon fiber operating room (OR) table rail.

FDAMay 18, 2023Nationwide• Baxter Healthcare Corporation

PRO Vibe Alloy Stems (Shimano) – crash risk (2023)

This recall involves PRO Vibe Stem (Alloy) model black bicycle stems for road bicycles. The PRO Vibe stems were sold separately and installed by bicycle stores. The recalled stems have a silver 'V' logo on the faceplate of the stem and the forward-facing mounting bolts.

CPSCMay 18, 2023Nationwide• Shimano Europe B.V., of the Netherlands

Aptio Automation SRM (Siemens) – Test Result Firmware Error (2023)

A firmware error may lead to an incorrect association of test result(s) to a sample ID and therefore to an incorrect patient result. The mis-association of test results, or a delay in testing, may occur when all the conditions listed below occur within a few milliseconds timeframe of each other: - The SRM module is releasing a sample tube (Tube A) just placed into the carrier - Another sample tube (Tube B) is erroneously not diverted into the SRM module buffer - There is divert gate malfunction and a narrow timing window Only in this specific scenario, Tube A may be released by the module as Tube B due to a miscommunication between the module firmware and the Automation software without a unique error message being generated. The Automation System loses the traceability of Tube A. It manages both Tube A (incorrectly identified as Tube B) and the real Tube B according to the pending test orders (not yet performed) on Tube B.

FDAMay 16, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.