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Product Recalls in Texas

All product recalls affecting Texas.

Includes nationwide recalls (tagged “Nationwide”) and recalls with Texas in the distribution area.

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Showing 2341–2360 of 34535 recalls

GYN Laparoscopy Pack (AVID Medical) – Visualization System Error (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Laparoscopic Prostatectomy (AVID Medical) – Visualization System Error (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

CT Da Vinci Kit (Avid Medical) – Visualization System Discoloration (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Laparoscopic GYN (AVID Medical) – Visualization System Error (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Lap Chole Pack (AVID Medical) – Visualization System Error (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Caphosol Artificial Saliva (Recordati) – Stability Test Concern (2025)

Out of specification stability test result for the Caphosol B solution from process validation lots

Moderate

FDAJun 11, 2025Nationwide• RECORDATI RARE DISEASES INC.

Laparoscopic Tray (Avid Medical) – Visualization System Discoloration (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

General Robotic Pack (Avid Medical) – Visualization System Discoloration (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Cardiac Robot Pack (Avid Medical) – Visualization System Discoloration (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Endosee Convenience Kit (CooperSurgical) – Iodine Pouch Labeling (2025)

The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.

Moderate

FDAJun 11, 2025Nationwide• CooperSurgical, Inc.

Asprire Cristalle Mammography (Fujifilm) – Unapproved Software (2025)

Devices had an unapproved slabbing software function enabled for use.

Low

FDAJun 11, 2025Nationwide• FUJIFILM Healthcare Americas Corporation

General Laparoscopy Tray (Avid Medical) – Visualization System Discoloration (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

GYN Robotic Pack (AVID Medical) – Visualization System Error (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Da Vinci Uro/Prostate Pack (Avid Medical) – Visualization System Discoloration (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Major Thoracoscopy Basin (AVID Medical) – Visualization System Error (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Pack General Robotic (AVID Medical) – Visualization System Error (2025)

CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Low

FDAJun 11, 2025CA, IL, MD +4 more• AVID Medical, Inc.

Famciclovir Tablets 500mg (Macleods) – Foreign Substance Found (2025)

Presence of Foreign Substance- Black hair strand found attached to a tablet in a sealed bottle.

Class IIILow

FDAJun 11, 2025Nationwide• Macleods Pharmaceuticals Ltd

Mercedes-Benz GLC 300 (Mercedes-Benz) – Headlight Cap Missing (2025)

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2023 GLC 300 and GLC 300 4MATIC vehicles. The headlights are missing adjustment prevention caps, which can allow the headlights to be improperly adjusted. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

High

NHTSAJun 11, 2025Nationwide• MERCEDES-BENZ