metal Recalls

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

Olympus SOLTIVE Pro Laser System Recall 2026 — 32 Units Worldwide

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 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.

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.

Olympus Everest Bipolar Cutting Forceps Recalled Worldwide for Welding Defect (164 Units, 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.

King Harvest Balsamic Hummus Recalled for Aluminum Shards in 326 10oz Tubs (2026)

King Harvest Roasted Red Pepper Hummus Recalled for Aluminum Pieces in 683 Containers (2026)

Pacific Coast Fresh CO Recalls King Harvest Sundried Tomato Hummus Over Aluminum Pieces (2026)

Pacific Coast Fresh CO Recalls King Harvest Spinach Hummus 2026 for Aluminum Fragments

Pacific Coast Fresh Co. Recalls King Harvest Jalapeno Hummus for Aluminum Pieces (2026) — 760 Units

King Harvest Black Olive Hummus Recalled for Aluminum Pieces in 319 Containers (2026)

Medline Sterile Radiology Procedure Kits Recalled for Sterility Breach (2026)

There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.

Mentor Texas CPX 4 US Breast Tissue Expanders Recall 2026

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Mentor Texas LP Recalls CPX 4 US Breast Tissue Expanders with Suture Tabs (2026)

Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.

Molded Products MPC-130 See Luer Cap Set Recalled for High-Risk Assembly Issue (2026)

Molded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the threaded sleeve not being engaged and becoming un-attached.

Olympus Biopsy Valves in Medline Thoracic Robotic Kits Recalled for Rubber Fragments (14,379 Kits,

Medline Recalls 14,379 Olympus Biopsy Valve Kits in 2026