Health & Personal Care Recalls

Spacelabs Healthcare 91496 Multi-parameter Module Recall Affects 1,790 Units Worldwide (2026)

Medline NAMIC Angiographic Syringe Recall Affects 17,902 Kits 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 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 Syringes Recalled in 439 Kits for Unwind Risk (2026)

Medline Industries, LP recalled 439 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans worldwide distribution including the US, Puerto Rico, and multiple international markets.

Medline NAMIC RA Syringe Adaptor Recall Aims to Prevent Connection Failures in 60 Kits (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 RA Syringes Recalled in 1698 Kits for Unwinding 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.

Medline NAMIC RA Syringe Recall: 108 Units Worldwide for Unwinding Adaptor (High Risk)

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 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 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 Syringe Recall for 1.75 Million Kits Over Adaptor Unwinding 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.

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.

Medline NAMIC Angiographic Adaptor Syringes Recalled in Class I Action for Rotation Unwinding Risk

Medline Industries, LP recalled 594 medical convenience kits worldwide, including NAMIC Angiographic Rotating Adaptor syringes, due to a potential unwinding of the syringe adaptor that can cause a loose connection or disconnection with the 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.

Medline NAMIC Angiographic RA Syringe Recall Expands to 966 Kits 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.

Macleods Pharma USA Recalls 1,315 Levothyroxine 150 mcg Tablets (2026)

Synthes Bone Taps Recall 33-Unit Lot Swap Causes Incorrect Threading (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.

Olympus Recall: 93 PKS Cutting Forceps Over Welding Defects (2026)

Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use.