All Recalls

92,900 total recalls in our database

Fractures and breakages in packaging trays and Tyvek covers, which may result in a sterility breach

Jul 1, 2024 Diagnostic Equipment Nationwide View Details →

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

Apr 8, 2024 Diagnostic Equipment Nationwide View Details →

CADD-Solis Ambulatory Infusion Pumps, with software versions before v4.3, may have the following issues:1. Upstream Occlusion, 2. Stop and Power Keys Unresponsive, 3. Manual Mode Air Detector, 4. Single Bubble Air Detection, 5. Error Codes Not Displayed at Power Up, 6. Audible Alarm, 7. Low Sensitivity Air in Line Detection Threshold, 8. PharmGuard Server Password. Smiths Medical corrected many of the issues included in this notification in previous software updates and the corrections were carried forward into all subsequent software releases. Please ensure you have the most recent CADD software (v4.3 - 2023) installed on your pumps.

Feb 27, 2024 Infusion Pumps View Details →

GE HealthCare has become aware that for certain MR systems, the system predicted B1+RMS value can exceed the B1+RMS user prescribed limit when scanning in Low SAR Mode and the following two conditions are met: 1. 2D FSE T2 FLAIR OR T2 FLAIR Propeller imaging sequence is selected, AND 2. the Optimized T2 FLAIR sequence option is turned off OR not included in the MR configuration. If this occurs, it can result in overheating of an MR conditional implant.

Jun 14, 2024 Diagnostic Equipment View Details →

The CADD Solis VIP Ambulatory Infusion Pump is indicated for the following uses: " For intravenous, intraarterial, subcutaneous, intraperitoneal, perineural, surgical site, epidural space, or subarachnoid space infusion.

Feb 27, 2024 Infusion Pumps View Details →

GE HealthCare has become aware that for certain MR systems, the system predicted B1+RMS value can exceed the B1+RMS user prescribed limit when scanning in Low SAR Mode and the following two conditions are met: 1. 2D FSE T2 FLAIR OR T2 FLAIR Propeller imaging sequence is selected, AND 2. the Optimized T2 FLAIR sequence option is turned off OR not included in the MR configuration. If this occurs, it can result in overheating of an MR conditional implant.

Jun 14, 2024 Diagnostic Equipment View Details →

Finger-Ease Guitar String Lubricants

Chem-Pak Inc., of Martinsburg, West Virginia

🏠 Consumer Products Class II - Moderate

The recalled guitar string lubricant contains a contaminant, posing a risk of skin irritation.

Aug 8, 2024 Other Consumer Products Nationwide View Details →

Slide-in Electric Ranges

Samsung Electronics America Inc., of Ridgefield Park, N.J.

🏠 Consumer Products Class I - Dangerous

Front-mounted knobs on the ranges can be activated by accidental contact by humans or pets, posing a fire hazard.

Aug 8, 2024 Other Consumer Products Nationwide View Details →

SMEG Refrigerators

Unknown Manufacturer

🏠 Consumer Products Class II - Moderate

The refrigerator door can detach and fall off, posing an injury hazard.

Aug 8, 2024 Furniture Nationwide View Details →