Medline

Medline medical procedure kits containing Stryker's Strykeflow 2 Suction Irrigators are being recalled due to a 2024 design change. The change allows irrigation solution to leak into the handpiece and battery pack during use, and some devices have emitted vaporized saline that resembles smoke. No injuries have been reported.

Medline medical procedure convenience kits containing Stryker's Strykeflow 2 Suction Irrigators have a design flaw that allows irrigation solution to leak into the handpiece and battery pack during use. Some devices have leaked fluid or emitted vaporized saline that may resemble smoke during procedures.

Medline medical procedure kits containing Stryker Strykeflow 2 Suction Irrigators may leak or emit vaporized saline during surgery due to a 2024 design change. The irrigation solution can travel into the handpiece and battery pack, potentially causing device malfunction or creating a smoke-like vapor in the surgical field.

Medline medical procedure kits containing Stryker Strykeflow 2 Suction Irrigators have a design flaw that allows irrigation fluid to leak into the handpiece and battery pack during use. Some devices have leaked or released vaporized saline that may resemble smoke. This affects specific thoracic and cardiac robotic surgery kits distributed nationwide.

Medline surgical kits containing B. Braun IV Administration Sets have been recalled because the check valve components may become stuck in the open or closed position. This could affect fluid flow during medical procedures. The recall affects four specific surgical kit types distributed nationwide.

Medline kits containing B. Braun IV administration sets have been recalled because the check valve components may become stuck in either the open or closed position. This could affect proper fluid delivery through the IV line. The affected kits are labeled as Neuro Angio Pack with SKU DYNJ38935, lot number 25IBC144.

Medline kits containing B. Braun IV Administration Sets may have check valve components that can become stuck in the open or closed position. This could affect proper fluid delivery during IV administration. About 1,725 units are affected nationwide.

Medline pre-op kits containing B. Braun IV administration sets have been recalled because the check valve components inside can get stuck in either the open or closed position. This could affect proper fluid delivery during medical procedures. No injuries have been reported to date.

Medline has recalled five IV starter kits that contain B. Braun IV administration sets. The check valve components in these sets may become stuck in the open or closed position, which could affect proper IV fluid delivery. No injuries have been reported so far.

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Medline kits labeled DR HOLCOMB FACIAL PACK (SKU DYNJ54488A) contain B. Braun IV Administration Sets with check valve components that may become stuck in the open or closed position. This can prevent proper fluid flow during IV administration. The recall affects 16 units distributed nationwide.

Medline kits containing B. Braun IV Administration Sets have been recalled because the check valve components may get stuck in either the open or closed position. This could affect how medication or fluids flow through the IV line. No injuries have been reported, but the sets should not be used.

Medline surgical kits containing B. Braun IV administration sets may have check valve components that become stuck in the open or closed position. This could affect fluid delivery during medical procedures. About 96 kits are affected.

Medline Deluxe Pre Op Kits containing B. Braun IV Administration Sets may have check valve components that stick in the open or closed position. This could affect the proper flow of intravenous fluids during medical procedures. The issue affects specific lot numbers distributed nationwide.

Medline has recalled eight models of cardiac surgery kits that contain B. Braun IV administration sets. The check valve components in these sets may become stuck in either the open or closed position, which could affect fluid delivery during surgery. No injuries have been reported.

Medline kits containing B. Braun IV administration sets have been recalled because the check valve components may become stuck in the open or closed position. This could prevent proper fluid flow during medical procedures. The recall affects 10 units distributed nationwide.

Medline Industries is recalling multiple models of Hudson RCI oxygen masks because the tubing can disconnect during use. If this happens, oxygen delivery stops, which can delay patient care and cause breathing problems that may require medical intervention.

Medline Industries' sterile Kelly forceps (5.5 inch, Item DYNJ04048) may have packaging seals that don't hold properly. If the seal fails, the sterile barrier is broken, which could allow bacteria or other germs to contaminate the instrument and increase infection risk if used.

Medline Industries sterile surgical scissors (5.5", Item DYND04000, Lot 2023102590) may have weak packaging seals that could break during storage or handling. If the sterile packaging fails, the scissors could become contaminated and increase infection risk if used in surgery or medical procedures.

Medline Industries is recalling DEXLOCK Achilles Repair Implant Kits (model MAKT4520, lot 19019) because the drill bit can fuse to the drill guide during surgery. This can delay the procedure while a replacement drill bit and guide are retrieved. No patient injuries have been reported.

Medline has found that Quick Strip Fabric Sterile Adhesive Bandages (1" x 3") may have open or damaged seals on their packaging. When the seal is compromised, the sterility of the bandages inside cannot be guaranteed. This affects all lots of the product.

Medline Industries has recalled all lots of Quick Strip Fabric Sterile Adhesive Bandages (0.75" x 3", Item Number NON25650QS) because the packaging seals may be open, which could allow bacteria or other contaminants to reach the bandages and compromise their sterility. No injuries have been reported.

Medline discovered that Fur Friends Plastic Sterile Adhesive Bandages (0.75" x 3") may have open or damaged seals in their packaging. This damage could allow bacteria or other contaminants to reach the bandages, making them non-sterile even though they are labeled as sterile. The issue affects all lots of the product.

Medline Industries has recalled all lots of Quick Strip plastic sterile adhesive bandages (1" x 3") because some packages may have open seals that could allow bacteria or contamination inside. This affects over 4 million units distributed in the US, Guam, Canada, and the UAE. No injuries have been reported.

Medline Industries identified that Quick Strip Plastic Sterile Adhesive Bandages (0.75" x 3") in all lots may have packaging seals that did not close properly. This means the bandages may not be sterile and could be contaminated. No injuries have been reported.

Medline discovered that some packages of Curad Quick Strip Fabric Bandages (item CUR1930P, 3/4" x 3") may have unsealed packaging, which could allow bacteria or contaminants to enter and compromise the sterility of the bandages. The issue affects all lots of these bandages.

Medline discovered that bandage packages may have open seals, which can allow bacteria and germs to contaminate the sterile bandages inside. This affects all lots of CURAD Touch-Free and Quick-Strip Bandages in the 0.75" x 3" size. No injuries have been reported so far.

Medline is recalling specific batches of Medline Perfusion Syringes (model DYNJ39223C) that contain BD Luer Tip Caps. BD's testing found that certain tip cap trays failed biocompatibility tests, meaning the plastic may cause skin irritation, allergic reactions, or other adverse effects if it contacts patients during use. No injuries have been reported so far.

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.