Health & Personal Care Recalls

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 Spectrum Central Venous Catheter Tray Recalled for Expired Shelf Life Labels (2026)

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."

Cook Medical Recall: Cook Staged Extubation Set Labeled with Expired Dates in 2026 Class II Recall

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.

Cook Medical CTO-18 Micro Wire Guide Recall Affects 75 Units Over Expired Dating (2026)

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.

Tomum Minoxidil Hair Serum Recalled Over Child Poisoning Risk

Koven Technology BiDop 3 Pocket Doppler ES-100V3 Recalled for Fetal Labeling Issue (2026)

Product labeling includes a fetal indication for use that is not cleared under its 510(k).

Philips Azurion 7 M20 X-ray System Recall Affects 5,167 Units Worldwide (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 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 FD10 OR Table Recalled for Intermittent X-ray Activation (2 Units, 2026)

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

KC Pharmaceuticals Recalled Sterile Eye Drops AC 182,424 Bottles Nationwide (2026)

Lack of Assurance of Sterility

Philips ALLURA Xper FD10/10 Imaging System Recalled for Intermittent X-ray Activation (112 Units)

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

Philips Azurion 5 M12 X-ray System Recall 2026: 345 Worldwide Units Affected

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

Oxoid Microbact 12L Kit 20 Tests Recalled for Misidentification Risk (2026)

Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to inconclusive result from ambiguous color reactions in wells.

Philips Azurion 7 B20 Interventional X-ray System Recall for 1,523 Units (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 Biplane OR Table Recall for 4 Units Over Intermittent X-ray Activation (202

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 M12 Recall for Intermittent X-ray Imaging (298 Units Worldwide, 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 FD20/10 Recall Affects 85 Imaging Systems in 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 5 M20 Recall: 920 Imaging Systems Worldwide 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 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.