tip over risk Recalls

17 Stories Furniture Dressers Recalled Over Tip-Over Risk

LIVEHOM Dressers Recalled Over Tip-Over Hazard Risk

LIVEHOM recalled 11-Drawer Dressers on March 12, 2026, due to tip-over hazards. The recall affects dressers sold on Amazon that can pose serious risks to children. Consumers must stop using these dressers immediately and contact the company for a full refund.

Cook Incorporated recalls Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set for Expired-

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

Cook Medical Spectrum Central Venous Tray Recalled Over Expired Shelf-Life Labels (2026)

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

Cook Medical Spectrum Central Venous Catheter Sets Recalled for Expired Shelf-Life Labels (2026)

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

Cook Medical Multipurpose Drainage Catheter Recalled Over Expired Labeling in Lots G29775

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

Cook Medical Approach CTO-12 Micro Wire Guide Recall Affects 49 Units for Expired Shelf-Life Labels

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 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.

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.

Philips Allura Xper FD20/15 OR Table Recall for 8 Units Worldwide in 2026

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

Medline Angiographic Control Syringe Recall for 192,690 Units Over Rotating Adaptor Hazard (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.

Medline NAMIC Angiographic Rotating Adaptor Syringe Recall Affects 762 Units Worldwide (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.

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 Rotating Adaptor Syringes Recalled in 82 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 Rotating Adaptor Syringes Recalled in 2,980 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 Syringes Recalled Globally for Rotating Adaptor Unwinding Risk (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 Medical Convenience Kits Recalled Worldwide Over Rotating Adaptor Unwinding

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.

Trankerloop Baby Bath Seats Recalled Due to Drowning Risk

Trankerloop recalled baby bath seats on February 26, 2026. The seats pose a drowning risk due to instability. Consumers should stop using them immediately and seek a refund.

Synthes 2.4V Bone Tap Locking Screw Tap 90mm Recall for 77 Units Nationwide (2026)

A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.