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Showing 741–760 of 22584 results

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Celsite BabyPort Set (B.Braun) – Minor Injury Potential (2025)

The potential for minor injury such as damage to the vessel and/or tearing of the vessel wall.

FDAJul 21, 2025Nationwide• B.Braun Medical S.A.S. Celsa Lg Medical 30 avenue des Temps Modernes; Cs 10031 Chasseneuil du Poitou CEDEX France

STA Satellite (Diagnostica Stago) – Contamination Risk (2025)

Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen reagents in UFH and LMWH applications.

FDAJul 21, 2025Nationwide• Diagnostica Stago, Inc.

Ultra IABP Catheter Kit (Insightra Medical) – FDA Review Concern (2025)

Device contains indications for use and device compatibility claims that have not be reviewed and approved for safety and effectiveness by the FDA. Instructions for use are not consistent with product training.

Moderate

FDAJul 19, 2025Nationwide• Insightra Medical Inc

Altivate Reverse Wedge Reamer (DJO Surgical) – Kickback Risk (2025)

Their is a potential that the reamer may kick or bind up during or immediately prior to use.

FDAJul 18, 2025Nationwide

IPC Powerease System (Medtronic) – Driver Wobble Issue (2025)

Due to out of the box wobble of the driver.

FDAJul 17, 2025AZ, CA, CO +22 more• Medtronic Xomed, Inc.

Orthopedic Pack (O&M Halyard) – Sterility Compromise (2025)

Surgical drape packs may have open seals, which may compromise the sterility of the product.

FDAJul 17, 2025Nationwide• O & M HALYARD INC

SureStep Foley Tray System (Bard) – Labeling Inaccuracy (2025)

Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction

FDAJul 17, 2025Nationwide• C.R. Bard Inc

SureStep Foley Tray System (Bard) – Labeling Inaccuracy (2025)

Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction

FDAJul 17, 2025Nationwide• C.R. Bard Inc

ReQuest Measles IgM Test (Quest) – FDA Approval Missing (2025)

Measles IgM Test Kit lacks premarket approval or clearance.

FDAJul 17, 2025Nationwide• Quest International, Inc.

Pinnacle 3 TumorLOC (Philips) – Calculation Error (2025)

Due to software issue, Radiation Therapy Planning system may provide incorrect dataset calculations when performing the "Stopping Power Ratio" (SPR) ,

FDAJul 17, 2025Nationwide• Philips Medical Systems (Cleveland) Inc

Pentax Medical Video Processor (Pentax) – Image Discoloration (2025)

During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endoscope, the observed image can become reddish or dark. Users have observed smoke like steam and noted that the light guide at the tip is hot during use / after the endoscope is removed from the patient and may cause thermal injury to the patient s mucous membrane.

FDAJul 16, 2025AZ, CA, FL +17 more• Pentax of America Inc

Dynex Agility Sample Tips (Dynex) – Labeling Error (2025)

The internal label affixed to the sample tip rack is incorrectly labeled as reagent tip racks. When scanned by the Agility instrument, the tip rack is misidentified as a different tip type, rendering it incompatible with the system and preventing use which causes a delay in obtaining patient results.

FDAJul 16, 2025CA, FL, NJ +2 more• Dynex Technologies, Inc.

TOPS Inserter (Premia Spine) – Missing Pin Risk (2025)

Potential for missing pins at tip of inserter.

FDAJul 16, 2025Nationwide• PREMIA SPINE LTD Giborey Israel 7 Ramat Poleg Netanya Israel

Prosthesis Head B (Waldemar Link) – Labeling Inconsistency (2025)

Inconsistent size terminology and color coding used on labeling

FDAJul 15, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Chromophare Surgical Light (Stryker) – Coating Stress Lines (2025)

Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.

FDAJul 15, 2025Nationwide• Stryker Communications

Plastic Trial Head (Waldemar Link) – Labeling Inconsistency (2025)

Inconsistent size terminology and color coding used on labeling

FDAJul 15, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Medline ReNewal Catheters (Medline) – Particulate Contamination (2025)

Specific lots of reprocessed electrophysiology catheters may contain small residual particulates.

FDAJul 14, 2025Nationwide• MEDLINE INDUSTRIES, LP Northfield

Corin Operating Tables (Maquet) – Device Interference Risk (2025)

Under certain conditions, such as the simultaneous use of the operating table with other medical devices, including high-frequency (HF) surgical equipment, interference may occur that could prevent the device from performing as intended. If the issue occurs, the operating table is unresponsive to command from both the universal remote control and override panel.

FDAJul 14, 2025Nationwide• MAQUET GMBH Kehler Str. 31 Rastatt Germany

3mensio Workstation (PIE Medical) – Measurement Error (2025)

When fenestrated analysis with clock measurements is started in diagnostic bioimaging software (intended to measure/visualize cardiovascular structures) and the 12h position of a single clock is changed, other clock measurements are not updated relative to the new 12h position which may cause stent graft fenestrations at incorrect position, which may lead to blood flow disruption and tissue damage

FDAJul 14, 2025Nationwide• PIE Medical Imaging B.V. Demertdwarsstraat 8A01 Maastricht Netherlands

Spectrum IQ Infusion Pump (Baxter) – Grease Breakdown (2025)

Baxter has identified that certain pumps have potentially been released with the grease applied to the cam and motor gears that will break down quickly. The breakdown of the grease will lead to the device having insufficient or ineffective grease applied to the cam, which could lead to premature wear of the mechanism assembly, resulting in excessive therapy.

FDAJul 14, 2025AZ, FL• Baxter Healthcare Corporation

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