We pull official government recall records and translate each one into plain language: what happened, how serious it is, and the steps to take. No legalese.
Search by meaning, not just keywords — describe the product or the hazard and we’ll find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Philips recalls ALLURA Xper FD10F X-ray systems with system code 722002 due to potential failure to initiate X-ray imaging when using the wired foot switch.
Philips recalls ALLURA Xper FD20 Biplane or Table systems with specific serial numbers due to potential X-ray imaging failures when using the wired foot switch. Affected units may not initiate or intermittently produce X-rays, posing a risk of improper imaging during procedures.
Oxoid recalls Listeria identification kits that may show incorrect results due to ambiguous color reactions. Affected kits have specific lot numbers and may need replacement.
Angiodynamics recalls Soft-Vu Angiographic Catheter (SOFT-VU PT 4F X 65CM 038 NB 10SH) due to a defect preventing guidewire passage. This could cause complications during medical procedures.
Philips recalls Azurion 5 M12 X-ray systems with specific system codes due to potential failure to initiate X-ray imaging when using the wired foot switch. Affected units may require repair or replacement.
