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Advanced Research Medical, LLC

Advanced Research Medical, LLC Recalls

All product recalls associated with Advanced Research Medical, LLC.

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Recall Summary

Total Recalls

1000

Past Year

1000

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 4441–4460 of 21320 recalls

Advanced Research Medical Fusion System (Advanced Research) – blade shearing risk (2023)

Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Assembly during surgery.

Moderate

FDAMar 14, 2023Nationwide• Advanced Research Medical, LLC

Atovaquone Oral Suspension 750mg (Camber) – Microbial Contamination (2023)

Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.

Class IHigh

FDAMar 13, 2023Nationwide• Camber Pharmaceuticals Inc.

Quantum Perfusion Systems (Spectrum Medical) – bobbin lock fault (2023)

The ratchet and pawl had an out of tolerance geometry which exhibited as the left bobbin would not lock.

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Moderate

FDAMar 13, 2023Nationwide• Spectrum Medical Ltd. Harrier 4, Meteor Business Park Cheltenham Road East Gloucester United Kingdom

VITROS XT 7600 Integrated System (Ortho-Clinical Diagnostics) – MicroTip Pack Issue (2023)

MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip Pack Caps on VITROS 5600 and XT 7600 Integrated Systems, results may be delayed results if a pack becomes unusable

Moderate

FDAMar 10, 2023Nationwide• Ortho-Clinical Diagnostics, Inc.

MAKO RESTORIS MCK Baseplate Trial (Stryker) – Incorrect Size Marking (2023)

Ccertain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking

Moderate

FDAMar 10, 2023Nationwide• Howmedica Osteonics Corp.

VITROS 5600 Integrated System (Ortho-Clinical Diagnostics) – MicroTip Pack Issue (2023)

MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip Pack Caps on VITROS 5600 and XT 7600 Integrated Systems, results may be delayed results if a pack becomes unusable

Moderate

FDAMar 10, 2023Nationwide• Ortho-Clinical Diagnostics, Inc.

Stryker MAKO Baseplate Trial (Howmedica) – incorrect size marking (2023)

Certain lots of the Restoris MultiCompartmental Knee (MCK) Tibial Baseplate Trials contain product with incorrect size laser marking

Moderate

FDAMar 10, 2023Nationwide• Howmedica Osteonics Corp.

Daytrana 10mg Patch (Noven) – Delivery System Defect (2023)

Defective Delivery System: Out of specification for shear.

Class IIModerate

FDAMar 10, 2023Nationwide• Noven Pharmaceuticals Inc

Daytrana 15mg Patch (Noven) – Delivery System Defect (2023)

Defective Delivery System: Out of specification for shear.

Class IIModerate

FDAMar 10, 2023Nationwide• Noven Pharmaceuticals Inc

Daytrana 30mg Patch (Noven) – Delivery System Defect (2023)

Defective Delivery System: Out of specification for shear.

Class IIModerate

FDAMar 10, 2023Nationwide• Noven Pharmaceuticals Inc

Daytrana 20mg Patch (Noven) – Delivery System Defect (2023)

Defective Delivery System: Out of specification for shear.

Class IIModerate

FDAMar 10, 2023Nationwide• Noven Pharmaceuticals Inc

VITROS Anti-SARSCoV-2 Antibody Calibrators (Ortho-Clinical) – Calibration Levels (2023)

Incorrect Number of Calibrator Levels (2) Set for the VITROS Immunodiagnostics Products Anti-SARS-CoV-2 Total N Antibody Calibrators in Assay Data Disks (ADD), resulting in delayed patients results

Moderate

FDAMar 9, 2023Nationwide• Ortho-Clinical Diagnostics, Inc.

DigitalDiagnost C50 (Philips) – Spring Balancer Tension (2023)

If the PM for the telescopic carriage is not performed annually as defined in the Instructions for Use (IFU), the tension force of the spring balancer inside of the telescopic carriage will unavoidably decay through normal wear and tear; as a result there is a potential that the Ceiling Suspension of the DigitalDiagnost C50 system may descend inadvertently if power to the system is interrupted, and may result in injuries to patients and users

Moderate

FDAMar 9, 2023Nationwide• Philips North America Llc