Search U.S. Product Recalls Database

Showing 6381–6400 of 8393 results

Sort:

Olympus PowerSeal 5MM Sealer (Olympus) – Rotation Knob Issue (2022)

An out of specification component preventing the blue retention ring from keeping the rotation knob in place. This may result in a loose rotation collar and retention ring and cause delay of treatment

FDAAug 12, 2022Nationwide• Olympus Corporation of the Americas

EMPOWR Acetabular Liner (Unknown) – Implant Mix-Up (2022)

Hip liner implant boxes may contain knee inserts and knee insert boxes may contain hip liner implants, which may lead to implants not being available for surgeries, which may cause delays in surgery.

FDAAug 12, 2022Nationwide

Stay Informed

Search Product Recalls

Olympus PowerSeal 5MM Sealer (Olympus) – Rotation Knob Issue (2022)

EMPOWR Acetabular Liner (Unknown) – Implant Mix-Up (2022)

COVID Test Kit (American Contract Systems) – Incorrect Labeling (2022)

Olympus PowerSeal 5MM Sealer (Olympus) – Rotation Knob Issue (2022)

EMPOWER 3D Knee Insert (Unknown) – Implant Mix-Up (2022)

IMMULITE Thyroid Test (Siemens) – Negative Bias (2022)

GXL Acetabular Liners (Exactech) – Packaging Defect (2022)

Artis Icono X-Ray System (Siemens) – Hardware Issue (2022)

VenaCure EVLT Kit (Angiodynamics) – Fiber Dimension Problem (2022)

Artis Q X-Ray System (Siemens) – Hardware Issue (2022)

Artis Pheno X-Ray System (Siemens) – Hardware Issue (2022)

Early Bird Bleed Monitoring System (Saranas) – Device Power Fault (2022)

Dewei DNA/RNA Kit (Unknown) – FDA Authorization (2022)

COVID-19 Ag Test (Jiangsu Well) – Unauthorized Distribution (2022)

BioZorb LP Marker (Hologic) – Expiration Label (2022)

Boston Scientific Guider Softip (Boston Scientific) – Tip Curve Mismatch (2022)

Stryker USB Converter (Mako) – Potential Failure (2022)

CoViPoint COVID Test (GS Biomark) – FDA Authorization (2022)

PDS II Suture (Ethicon) – Material Error (2022)

MEGA Intra-Aortic Balloon (Datascope) – Dilator Size (2022)