Search U.S. Product Recalls Database

Showing 361–380 of 8389 results

Sort:

SAFE-T-FILL Tube Extender (ASP) – manufacturing process (2025)

Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.

FDASep 26, 2025Nationwide• ASP Global, LLC. dba Anatomy Supply Partners, LLC.

AART Gluteal Implant (DSAART) – specification deviation (2025)

Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.

Moderate

FDASep 26, 2025AZ, AR, CA +24 more• DSAART LLC

Stay Informed

Search Product Recalls

SAFE-T-FILL Tube Extender (ASP) – manufacturing process (2025)

AART Gluteal Implant (DSAART) – specification deviation (2025)

AART Silicone Carving Implant (DSAART) – specification deviation (2025)

Incisive CT (Philips) – movement control issue (2025)

CT 5300 (Philips) – movement control issue (2025)

Covidien Signia Reload (Unknown) – firing mechanism risk (2025)

Artegraft Collagen Vascular Graft (LeMaitre) – incorrect packaging (2025)

Cold Form Wrap (DJO) – microwave heating risk (2025)

MEGA Ballast Access Platform (BALT) – coating defect (2025)

Incisive CT Brazil (Philips) – movement control issue (2025)

HARMONIC FOCUS Shears (Stryker) – continuous activation (2025)

Sealing Unit for Trocars (Aesculap) – silicone fragment risk (2025)

BD Phoenix M50 Instrument (BD) – credential breach (2025)

BD EpiCenter System (BD) – credential breach (2025)

BD MAX System (BD) – credential breach (2025)

BD Veritor Connect Software (BD) – credential breach (2025)

ZipTight AC Joint Implant (Biomet) – missing component (2025)

Klassic BiPolar Head (Total Joint) – sterility compromise (2025)

BACTEC Blood Culture System (BD) – credential breach (2025)

DxFLEX Flow Cytometer (Beckman) – software crash risk (2025)