Every recall we track for Covidien, LP — 111 in all — plus the complaints and injury reports the public filed about them.
Covidien recalls Dermalon 4-0 Blue 75cm sutures with possible packaging tears that could cause infection. Affected items have specific lot numbers and model codes. Consumers should check their product details.
Covidien recalls Surgipro SP-623 sutures that may have torn packaging, risking infection or vision loss during surgery. Affected products include specific model and lot numbers.
Covidien recalls V-Loc 90 Absorbable Wound Closure Devices with possible perforations in sterile packaging that could cause infection or vision loss during surgery.
Covidien recalls Surgipro II S8698GX sutures due to possible perforations in sterile packaging that could cause infection or vision loss during surgery.
Covidien recalls V-Loc 180 Absorbable Wound Closure Devices with possible packaging perforations that could cause infection or vision loss during surgery.
Covidien recalls EndoStitch Polysorb Single Use Loading Units with product numbers 170053 and 170071 due to potential pouch holes compromising sterility. Affected units may not protect the product from environmental exposure.
Covidien recalls Signia Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin) with CFN SIGSDL45CTVT due to potential uncontrolled motion from a manufacturing issue.
Covidien recalls specific Signia small diameter curved tip intelligent reload devices due to potential uncontrolled motion from manufacturing issues. Affected units may require replacement to prevent internal component movement.
Covidien recalls specific lots of Chameleon PTA Balloon Catheter with Injection Port due to failure in balloon pressure testing. Affected units include 5mm to 12mm sizes with listed lot numbers and UDI-DI codes.
Covidien recalls Tri-Staple 2.0 Black Reinforced Intelligent Reload cartridges for potential poor staple formation, which may delay surgery. Affected units have specific model and lot numbers.
Covidien recalls Palindrome Precision H Chronic Catheter Kits with potential heparin coating defects. These kits may not provide intended anticoagulant benefits, risking clot formation during hemodialysis procedures.
Covidien recalls Palindrome Precision HSI Chronic Catheter Sport Packs due to potential missing heparin coating, which may reduce treatment benefits. Affected units have specific model and lot numbers.
Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T10BTS) due to potential seal disengagement when used incorrectly with mesh products. Affected units include specific lot numbers.
Covidien recalls Auto Suture Structural Balloon Trocar (OMS-T10SB) due to potential seal disengagement when mesh products are used incorrectly. Affected units include specific lot numbers. Consumers should contact for details.
Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T10BTNL) due to potential seal disengagement when mesh products are used incorrectly. Affected units include specific lot numbers and serials.
Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T12BTNL) due to potential seal disengagement when used incorrectly with mesh products. Affected units include specific lot numbers and serial codes.
Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T10BTSNL) due to potential seal disengagement when mesh products are used incorrectly. Affected units include specific lot numbers and serials.
Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T12BT) due to potential seal disengagement when mesh products are used incorrectly. Affected units include specific lot numbers. Consumers should stop using if they have the product.
Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T10BT) due to potential seal disengagement when used incorrectly with mesh products. Affected units have specific lot numbers. Stop using immediately if you have this device.
Covidien recalls specific Signia Small Diameter Curved Tip Intelligent Reloads (Model SIGSDS30CTVT) due to potential uncontrolled articulation during use, which could disrupt staple lines. Affected units include certain lot numbers and UDI/DI codes.
Covidien recalls Signia Small Diameter Curved Tip Intelligent Reload Model SIGSDS30CTVT due to potential uncontrolled articulation during use, which could disrupt staple lines. Affected users should contact for details.
Covidien recalls Sofsilk Braided Silk sutures (Product S-2782K) due to potential tensile strength reduction from excessive ethylene oxide sterilization cycles, which may cause wound complications.
Covidien recalls specific lots of Sofsilk Braided Silk sutures due to gamma sterilization exceeding approved levels, which may weaken sutures over time and cause wound dehiscence or severe bleeding.
Covidien recalls specific Surgilon nylon sutures due to gamma sterilization exceeding approved levels, potentially weakening sutures over time and causing wound dehiscence or severe bleeding.
Covidien recalls 30 Violet Absorbable Tacks for potential sterility breach due to packaging issues. Affected units may compromise surgical product safety.
Covidien recalls Palindrome Chronic Catheter Kits with incorrect 28cm catheters labeled as 23cm. Check your kit's label for correct implant length to avoid complications.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion due to excessive silicone lubricant. Affected units may cause delays in treatment or blood clots.
Covidien recalls specific dialysis catheters with potential occlusion from excessive silicone lubricant, risking blockage and treatment delays. Affected units include model 8888345611HP with certain lot numbers.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls 12 Fr high pressure triple lumen dialysis catheters with potential occlusion from excessive silicone lubricant. Affected units may cause treatment delays or blood clots. Stop using immediately.
Covidien recalls 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion due to excessive silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls specific dialysis catheters with potential occlusion risk from silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls specific 12Fr high-pressure triple lumen dialysis catheters due to silicone lubricant causing tip occlusion, potentially leading to treatment delays or complications.
Covidien recalls MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheters with potential silicone lubricant occlusion causing blockages, delays in treatment, or blood clots.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion due to excessive MDX lubricant. Affected units may cause blockages or clotting risks during dialysis treatment.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause delayed treatment or clotting risks.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheters with occlusion risk from excessive silicone lubricant. Affected units may cause treatment delays or blockages.
Covidien recalls specific 12 Fr high-pressure triple lumen dialysis catheters due to silicone lubricant causing tip occlusion, potentially leading to treatment delays or complications.
Covidien recalls specific dialysis catheters due to silicone lubricant causing blockages that may delay treatment or cause complications. Affected units have lot numbers 2131200173, 2133700237, 2200400273, 2200400290.
Covidien recalls MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheters with potential occlusion due to excessive lubricant. Affected units may cause treatment delays or complications.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheters with potential occlusion due to excessive silicone lubricant. Affected units may cause blockages or clotting if used.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion due to excessive silicone lubricant. Affected units may cause blockages or clotting risks during dialysis.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause delays in treatment or blood clots.
Covidien recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause treatment delays or complications.
Covidien recalls 12 Fr High Pressure Triple Lumen Acute Dialysis Catheters with potential occlusion from excessive silicone lubricant. Affected units may cause blockages or blood clots.
Covidien recalls VersaOne Reusable Positioning Cannula 8mm Standard (Model RC8STS) due to potential metal shavings from welding. Affected units have specific serial numbers. Stop using immediately to avoid injury.
Covidien recalls VersaOne Reusable Positioning Cannula 12mm Standard (RC12STS) due to potential metal shaving at weld point. Affected units have specific serial numbers and UDI-DI codes.
Covidien recalls VersaOne Reusable Positioning Cannula 11mm Standard (Model RC11STS) due to potential metal shavings from welding. Affected units have specific serial numbers. Consumers should check their product details.
Covidien recalls specific mild chromic gut absorbable sutures due to potential unsterile product from supplier calibration issues. Use may cause infection or vision loss in eye procedures. Affected items have GTINs and specific lots.
Covidien recalls specific Plain Gut Absorbable Sutures due to potential unsterile product from supplier calibration issues. Use may cause infection or vision loss in eye sutures. Affected lots and GTINs listed.
Covidien recalls specific sutures due to potential unsterile product from supplier calibration issues. Use may cause infection or vision loss in eye surgeries. Check product codes to see if affected.
Covidien recalls Step Bladeless Trocars with possible unsterile product due to supplier calibration issues. Use may cause infection or vision loss in eye sutures. Affected units include specific product numbers and lots.
Covidien recalls Tri-Staple 2.0 Black Intelligent Reload (SIG60AXT) due to potential broken sled vane causing misfire and tissue damage. Affected lots may lead to delayed treatment, bleeding, or death.
Covidien recalls Parietex Composite Mesh with Absorbable Collagen Film due to risk of delayed treatment, adhesions, and implant failure. Affected patients should contact for guidance.
