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Baxter Corportation is issuing a recall for certain lots of the Minicap. These devices are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals.  Baxter is expanding the urgent medical…

The Nobil Grip (product numbers 0102000 and 0102000-3) secondary package for lot 21v0089 and 194397, is labeled with an incorrect expiration date.  Recall start date: February 4, 2023

A portion of the products in the specific lots identified above were packaged and marked (i.e., laser etched) incorrectly, specifically: catalog no. gl11, lot number d22xbb may be marked (i.e., laser etched), packaged, and labeled as catalog no. gl31,…

Zimmer Biomet is conducting a medical device correction to update the compatibility matrix as referred to in the instructions for use (IFU) for the CoCr Femoral Head XS. The update is to remove the compatibility with the Epsilon Durasul Constrained …

It was discovered that the Instructions for Use (IFU) of the Tracoe Experc dilation set, ref 520, has not been included in the product scope of the Tracoe Experc sets for Vario, Twist and Twist Plus. Recall start date: February 01, 2023

On Delfia Inducer bottles (2 kit lots), the label is placed too low preventing the Delfia Xpress instrument level sensor to detect the Delfia inducer liquid level. Because of that the instrument does not give an 'inducer bottle soon empty' warning at…

Stryker has identified that there is a potential that the affected device was shipped with the incorrect language configuration. Recall start date: January 26, 2023

During the investigation process of customer complaints, Lina has become aware of a safety issue in relation to the use of an obsolete version of an accompanying document. The use of an obsolete customer quick reference guide resulted in the incorrect…

BVI has received a complaint from a customer that catalog # 376630 of the Beaver Edgehead Stiletto/Mvr knife 0.90 mm Straight (20g), a component of the Readpak kit (cat:584896, lots:6054175,6053035), was shipped with an open head. BVI is recalling the…

These pediatric nasal oxygen cannulas had sticky film when package was opened -  expired product or nearly expired product released placticizer film. Recall start date: December 05, 2022

Siemens Healthcare Diagnostics Inc. has confirmed through customer complaints the potential for functional sensitivity to not meet instructions for use (IFU) claims with the kit lots listed in table 1. Additionally, immulite thyroglobulin control module…

Stryker is notifying airo truct customers that we will be highlighting certain information that is already in the airo truct user manual on labels affixed to the airo truct unit itself. Stryker received one report of an injury to an untrained user that…

Unsealed edge of blister package containing individual GLC devices. Device may not meet label claims for sterility. One complaint has been reported with the unsealed edge of the blister package containing individual GLC devices. There were no adverse…

This recall addresses a product concern regarding the drapes in the kit. The supplier (3M) decided to recall the drapes in the kit because it was confirmed that the liner on the adhesive component of the affected drapes is difficult to remove without…

Medline Industries, lp is issuing a safety alert for custom procedure packs containing sterile blades due to the potential of the blade puncturing the outer foil layer of the sterile packaging. Recall start date: November 21, 2022