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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

The firm has become aware of a potential issue with the AIA-360 analyzer that could prevent the table home sensor from detecting the table home position. If the malfunction with the table home sensor occurs on the AIA-360, the sensor board may need to be replaced. If the home sensor fails to detect the home position, the AIA-360 analyzer will cease to function and will be unavailable for use. If this issue occurs, there may be a delay in testing and reporting patient test results. Tosoh has received three (3) complaints related to this issue with no serious injuries reported.

Mar 22, 2017 Diagnostic Equipment Nationwide View Details →

RBC Reagent failure. High fluorescent counts during RBC Reagent + Diluent QC check that will result in failed QC check, preventing user from testing patient samples for RBC.

Feb 7, 2018 Diagnostic Equipment Nationwide View Details →

Mislabeled Labeled Avenir M¿ller Stem size 1, the stem inside the packaging is an Avenir M¿ller Stem size 2 .

Oct 31, 2018 Implants & Prosthetics View Details →

Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.

Oct 31, 2018 Surgical Instruments Nationwide View Details →

Inaccurate potassium results may be generated. When testing with control fluid and/or patient samples with low or reference range potassium concentration, elevated potassium results may be generated. When testing with samples with a high concentration of potassium, decreased potassium results may be generated

Sep 13, 2018 Other Medical Devices View Details →

In some situations the carousel position pin (locker) may cause the carousel upper plate to pop out and the carousel may then inadvertently move.

Nov 26, 2014 Implants & Prosthetics View Details →

Table may drift in the roll position while in use

Nov 6, 2018 Diagnostic Equipment Nationwide View Details →

Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.

Oct 31, 2018 Surgical Instruments Nationwide View Details →

Unintentional U-Arm movement

Nov 8, 2018 Infusion Pumps Nationwide View Details →

Software anomaly may incorrectly extend the on-analyzer stability time for a loaded VITROS Reagent.

Oct 19, 2018 Diagnostic Equipment Nationwide View Details →

Table may drift in the roll position while in use

Nov 6, 2018 Diagnostic Equipment Nationwide View Details →

Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.

Oct 31, 2018 Surgical Instruments Nationwide View Details →

Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.

Oct 31, 2018 Surgical Instruments Nationwide View Details →

A percentage of the products shipped in Smartscope single-box packaging may exhibit a broken package seal, thus having compromised sterility. There have been two reports of compromised sterility; however, all products packaged in Smartscope single-box packaging are at risk of a compromised product seal. Broken seal pouches compromise sterility and could increase the risk of infection if used.

Oct 17, 2018 Surgical Instruments View Details →