Philips Intera 1.5T Power/Pulsar, Magnetic Resonance System recall — FDA Z-1582-2024
Patient support table floor plate may be incorrectly installed.
Monitor U.S. medical device recall enforcement reports from the FDA. Review product descriptions, recall reasons, classifications, dates, recalling firms and distribution information where the FDA provides them.
22,877 detailed records are currently available in this category.
Patient support table floor plate may be incorrectly installed.
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Patient support table floor plate may be incorrectly installed.
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Patient support table floor plate may be incorrectly installed.
Patient support table floor plate may be incorrectly installed.
Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and P0561740 may contain a molding defect…
Degraded and unusable upon removal from the foil pouch due to exposed environmental conditions during transit and storage, compromising sterility
Patient support table floor plate may be incorrectly installed.
Patient support table floor plate may be incorrectly installed.
Patient support table floor plate may be incorrectly installed.
Patient support table floor plate may be incorrectly installed.
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Retrospective engineering analysis against current ISO standards for hoists has determined: 1. The device cannot physically perform at maximum documented weight specifications when a factor…
Patient support table floor plate may be incorrectly installed.
Patient support table floor plate may be incorrectly installed.
Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to exchange the device for…
Software has anomalies that have the potential to cause underdose, overdose, or delay in therapy which could lead to serious patient harm or death.
Insufficient welding leads to the heater cable becoming brittle and present with an error: ERROR 3481 HEATER UNABLE TO REACH TEMPERATURE; the instrument may stop, and the sample being…
The product does not meet sterility assurance level.
Medical device components were marketed without FDA clearance
Baxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical standards.
Medical device recall records can change as the FDA receives additional information. Check the official record identifier and current FDA information before making health or product-use decisions.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.