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.
794 recalls tagged with “infant product”.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Affected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max system.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook Medical recalled 1,872 units of Spectrum Central Venous Catheter Trays worldwide due to expiration dates labeling that exceed true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions."
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Cook Medical recalled 75 CTO-18 Micro Wire Guide devices distributed worldwide. The recall cites expiration date labeling that exceeds the true shelf life. Healthcare providers should stop using affected lots immediately and follow manufacturer instructions.

HALO Dream recalled its Magic Sleepsuit on March 5, 2026, after discovering a choking hazard. The recall affects specific batch codes PO30592, PO30641, and PO30685. Parents should immediately stop using these sleepsuits and seek a refund or replacement.
Product labeling includes a fetal indication for use that is not cleared under its 510(k).
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Lack of Assurance of Sterility
Lack of Assurance of Sterility