workplace Recalls

House of Flavors Chicago Vanilla Ice Cream Recall 4,880 Tubs Over undeclared Egg (2026)

Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords Recalled in 2026 Walmart Recall

Tainoki Fine Furniture Recalls 3 Office Chairs Over Fall Hazard (2026)

Straumann USA Recalls 13 Custom Abutment Ti RC for TAN Material Mix-Up (2026)

Cook Medical Thal-Quick Chest Tube Tray Recalled for Expiration Dates Exceeding Shelf Life

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical Wayne Pneumothorax Tray Recalled for Expired-Labeled Shelf Life (2026)

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Cook Medical Recall: Strange Bile Duct Stone Exploration Set Labeled with Expired Dates (Z-1784-2026

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Philips ALLURA Xper FD20 Recall for 5,084 Units Over Intermittent X-ray Imaging (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Allura Xper FD20/20 Recall 111 Systems Worldwide Over Intermittent Imaging (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Medical Systems Nederland recall 296 Allura Xper FD20/15 Imaging Systems Over Foot Switch Fl

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips ALLURA Xper FD20 OR Table Recalled Worldwide; 196 Units Affected (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Azurion 3 M15 Recall for 798 Units Worldwide Over Intermittent X-ray Imaging (2026)

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

Philips Azurion 7 B12 X-ray System Recalled for Foot Switch Imaging Failure (670 Units, 2026)

Philips recalls 670 Azurion 7 B12 X-ray imaging systems after finding the wired foot switch may fail to start imaging. The issue affects 106 US units and 564 in other countries. Hospitals should stop using the device and await manufacturer guidance.

Civco Medical Instruments Recalls 10 eTRAX Needle Sensor 16G for Aurora Trackers (2026)

There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.

Civco Medical eTRAX 14G Needle Sensor Recall for 5 Units (2026)

There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.

Civco Medical Instruments Recalls 21 eTRAX Needle Sensors for Aurora Trackers (2026)

There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.

GE Healthcare SIGNA Premier MRI Systems Recalled Worldwide for Ferrous Fittings Hazard (41 Units, 6)

Medline NAMIC Angiographic Adaptor Syringe Recall Expands Worldwide in 240 Kits (Class I)

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Medline NAMIC Angiographic Syringe Recall for 2,154 Kits Worldwide

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Medline NAMIC Angiographic Syringe Recalled Globally Over Rotation Adaptor Risk (2026)

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.