Recalls published in October 2025
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in October 2025, newest first.
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Class I · 1+ years ago
Medline Kits: 1) Valve Pack-Lf recall: The kits contain certain lots of cannula products where the catheter
The kits contain certain lots of cannula products where the catheter may not retain its shape.
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Class I · 1+ years ago
Siemens Medical Solutions USA, Inc Magnetom Skyra Fit BioMatrix recall: There is a potential for an ice blockage to form or currently exist within
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be…
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Class I · 1+ years ago
Medline Industries, LP Reprocessed Webster CS Catheter 10 Electrodes recall: Specific lots of reprocessed electrophysiology and ultrasound catheters
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual…
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Class I · 1+ years ago
Siemens Medical Solutions USA, Inc Magnetom Spectra as the following: 1. Magnetom recall: There is a potential for an ice blockage to form or currently exist within
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be…
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Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD10 OR Table recall: The BIOS battery may deplete faster than initially anticipated during
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the…
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Class II · 1+ years ago
Change Healthcare Radiology Solutions software version 14.2.2 recall: Due to software issue, radiology reports may not be fully displayed
Due to software issue, radiology reports may not be fully displayed when viewing.
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Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/20 OR Table recall: The BIOS battery may deplete faster than initially anticipated during
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the…
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Class II · 1+ years ago
Howmedica Osteonics Corp. 1. Exeter V40 Stem 44MM NO 2, Model/ recall: a potential product mix where the package labeled as Catalog Number
a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and…
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Class I · 1+ years ago
Siemens Medical Solutions USA, Inc Magnetom Lumina recall: There is a potential for an ice blockage to form or currently exist within
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be…
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Class I · 1+ years ago
Sterile Medline recall: Convenience kits labeled as sterile have not gone through the sterilization
Convenience kits labeled as sterile have not gone through the sterilization process.
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Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/10 recall: The BIOS battery may deplete faster than initially anticipated during
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the…
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Class I · 1+ years ago
Siemens Medical Solutions USA, Inc Magnetom Verio recall: There is a potential for an ice blockage to form or currently exist within
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be…
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Class II · 1+ years ago
Schiller, Ag Argus PB-3000, Reference Numbers: 1A.701307 recall: Vital sign monitoring instrument may trigger an error message during blood
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure…
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Class II · 1+ years ago
Getinge 88-Series Washer- Disinfector recall: Potential for device to overheat during operation if the circulation pressure
Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and…
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Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD20/15 recall: The BIOS battery may deplete faster than initially anticipated during
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the…
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Class II · 1+ years ago
Northeast Scientific Inc. NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy recall: Potential for breaches in the sterile barrier packaging
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
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Class II · 1+ years ago
Aesculap Elan 4 Fixed Duraguard Standard recall: Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long"
Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."
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Class II · 1+ years ago
Philips Medical Systems Nederland B.v. Allura Xper FD10 recall: The BIOS battery may deplete faster than initially anticipated during
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the…
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Class I · 1+ years ago
Medline Industries, LP Reprocessed Livewire Steerable Electrophysiology Catheter Item recall: Specific lots of reprocessed electrophysiology and ultrasound catheters
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual…
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Class I · 1+ years ago
Draeger, Inc. Brand Name: Atlan Product Name: Atlan A350 Model/ recall: The device either indicated a failure of the piston ventilator before use
The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
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Class II · 1+ years ago
ZAP-X recall: If the radiosurgery system triggers a proximity error message during a long
If the radiosurgery system triggers a proximity error message during a long gantry move (greater-than180 degrees), and a subsequent proximity error…
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Class II · 1+ years ago
MedicalCommunications GmbH Ashvins variant Heyex 2 / Heyex Pacs. Software Version recall: Potential that the measured value may be smaller than the actual area
Potential that the measured value may be smaller than the actual area.
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Class II · 1+ years ago
Northeast Scientific Inc. NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy recall: Potential for breaches in the sterile barrier packaging
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
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Class II · 1+ years ago
Northeast Scientific Inc. NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy recall: Potential for breaches in the sterile barrier packaging
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.