Search U.S. Product Recalls Database

Showing 1681–1700 of 1734 results

Sort:

HPV Control Panel (Microbiologics) – quality control issue (2025)

Internal quality control procedures were not followed correctly for the testing/release of three lots of 8234/8235. This resulted in the release of products that should have failed and been discarded. The concentration of one target (HPV 16 L1) was low enough to cause QC failures, no detection, or invalid results on some instruments and assays.

Moderate

FDAJan 20, 2025Nationwide• Microbiologics Inc

3M V.A.C. Wound Therapy System (KCI) – leak alarm issue (2025)

Due to increase in complaints related to leak alarms

Moderate

FDAJan 17, 2025Nationwide• KCI USA, INC.

Stay Informed

Search Product Recalls

HPV Control Panel (Microbiologics) – quality control issue (2025)

3M V.A.C. Wound Therapy System (KCI) – leak alarm issue (2025)

Homedics Leg Massager (Luyao Electronics) – packaging error (2025)

3M Prevena Plus Therapy Unit (KCI) – leak alarm issue (2025)

RayStation Planning System (RaySearch) – density uncertainty (2025)

Quantum Perfusion Blood Pump (Spectrum) – fluid leakage (2025)

Plato 17 Microcatheter (Scientia) – packaging seal breach (2025)

ASP BIOTRACE Auto Read (Unknown) – Incorrect Incubation (2025)

IntelliBridge EC10 Module (Philips) – alarm failure (2025)

IntelliVue Patient Monitor (Philips) – alarm failure (2025)

Sevoflurane Vaporizer (Getinge) – chemical degradation (2025)

MOSAIQ Oncology System (Elekta) – Image Offset Risk (2025)

Sertera Biopsy Device (Hologic) – Needle Separation (2025)

DeRoyal AMG Suction Connector (DeRoyal) – Seal Integrity (2025)

IntelliVue Patient Monitor (Philips) – Alarm Failure (2025)

Single Use Guide Sheath Kit (Olympus) – radiopaque tip risk (2025)

Infinity Central Station (Draeger) – Speaker Malfunction (2025)

Azurion 7 M20 (Philips) – Safety Issue (2025)

Allura Xper FD10C (Philips) – Safety Issue (2025)

Allura Xper FD20 (Philips) – Patient Fall Risk (2025)