Covidien, LP recalls
Every recall we track for Covidien, LP — 111 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 8 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Covidien, LP fell by more than half in 2025 (2, down from 14 in 2024). 7% rated “stop using now”.
All FDA recall records for Covidien, LP since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 1 | 8 | 0 | 9 |
| 2021 | 0 | 4 | 20 | 2 | 26 |
| 2022 | 5 | 10 | 0 | 0 | 15 |
| 2023 | 3 | 31 | 4 | 0 | 38 |
| 2024 | 0 | 8 | 5 | 1 | 14 |
| 2025 | 0 | 1 | 0 | 1 | 2 |
| 2026 (to date) | 0 | 2 | 4 | 0 | 6 |
What to do if you have a recalled Covidien, LP product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Covidien, LP recalls
27 shown- Lower riskMedical device
Covidien, LP recalls Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31
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.
CovidienJun 24, 2026 - Lower riskMedical device
Covidien, LP recalls Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;
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.
CovidienApr 15, 2026 - Use cautionMedical device
Covidien, LP recalls Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN:
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.
CovidienSep 25, 2025 - UnratedMedical device
Covidien LP recalls Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm x 75cm (CFN CH05-40-75US), 6mm x 40mm x 75cm (CFN
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.
CovidienSep 19, 2024 - Lower riskMedical device
Covidien, LP recalls Tri-Staple 2.0 Black Reinforced Intelligent Reload- Applications in abdominal, gynecologic, pediatric and thoracic
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.
CovidienApr 15, 2024 - Lower riskMedical device
Covidien LP recalls Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm) x 19 cm (Symmetrical Tip, Heparin Coating,
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.
CovidienMar 15, 2024 - Use cautionMedical device
Covidien, LP recalls Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BT
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.
CovidienFeb 28, 2024 - Use cautionMedical device
Covidien, LP recalls Signia" Small Diameter Curved Tip Intelligent Reload, Model SIGSDS30CTVT
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.
CovidienFeb 14, 2024 - Lower riskMedical device
Covidien, LP recalls Sofsilk Braided Silk sutures, Product Number S-2782K. Nonabsorbable, sterile, non-mutagenic surgical suture composed of
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.
CovidienJan 25, 2024 - Use cautionMedical device
Covidien LP recalls Surgilon Braided Nylon sutures: 88861919-31 SURGILON* 4-0 BLK 7X75CMPCT 88861919-41 SURGILON* 3-0 BLK 7X75CMPCT
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.
CovidienDec 21, 2023 - Stop using nowMedical device
Covidien LP recalls AbsorbaTack Absorbable Fixation Device 30 Violet Absorbable Tacks 5 mm- -intended for fixation of prosthetic material
Covidien recalls 30 Violet Absorbable Tacks for potential sterility breach due to packaging issues. Affected units may compromise surgical product safety.
CovidienNov 16, 2023 - Lower riskMedical device
Covidien LP recalls Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm
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.
CovidienAug 22, 2023 - Use cautionMedical device
Covidien LP recalls MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, IC Tray REF: 8888102004HP
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.
CovidienJun 28, 2023 - Lower riskMedical device
Covidien LP recalls VersaOne Reusable Positioning Cannula 11mm Standard, Model Number RC11STS
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.
CovidienMar 22, 2023 - Use cautionMedical device
Covidien, LP recalls Step Bladeless Trocars, 10 mm cannula and dilator with radially expandable sleeve and 5 - 10 mm reducer, Product Number
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.
CovidienMar 1, 2023 - Stop using nowMedical device
Covidien, LP recalls Tri-Staple 2.0 Black Intelligent Reload, Product Number SIG60AXT
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.
CovidienJan 25, 2023 - Lower riskMedical device
Covidien, LP recalls Parietex Composite Mesh Polyester with Absorbable Collagen Film, Horseshoe- Shaped, 9 x 8 cm (3.6" x 3.1"). Intended
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.
CovidienJan 11, 2023 - Use cautionMedical device
Covidien LP recalls MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter, Sterile, Single Use, Rx Only: 13.5cm, Straight
Covidien LP recalls specific models of MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheters due to potential fluid leakage in the hub. Affected units have model numbers and serial numbers listed in the recall notice.
CovidienDec 7, 2022 - Stop using nowMedical device
Covidien, LP recalls Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON* 2-0 BLK 75CM C16 88861915-71 SURGILON* 1 BLK
Covidien recalls Surgilon sutures with possible infection or vision loss risk if sterile pouch breaches during eye surgery. Check product codes to see if affected.
CovidienDec 2, 2022 - Use cautionMedical device
Covidien, LP recalls Endo Stitch V-Loc 180 Absorbable Reload, Models VLOCA004L, VLOCA006L, VLOCA008L, VLOCA204L, VLOCA206L, VLOCA208L,
Covidien recalls Endo Stitch V-Loc 180 Absorbable Reload models due to reports of needles breaking during endoscopic suturing, potentially causing delays in treatment, tissue injury, or foreign body reactions.
CovidienSep 28, 2022 - Use cautionMedical device
Covidien, LP recalls EEA Autosuture Circular Stapler with DST Series Technology, 25mm. Model Numbers EEA25, EEAXL25, EEA2535, and EEAXL2535.
Covidien recalls EEA Autosuture Circular Stapler models EEA25, EEAXL25, EEA2535, and EEAXL2535 due to potential staple guide disengagement causing tissue transection without staples.
CovidienMay 13, 2022 - Use cautionMedical device
Covidien, LP recalls SonarMed AirWave Monitor Kit (Monitor, Sensor Cable, Power Cord), Item Code AW-M0001. used with endotracheal tube (ETT)
Covidien recalls SonarMed AirWave Monitor Kit (AW-M0001) used with endotracheal tubes due to false alarm disconnections causing monitoring to stop without warning.
CovidienDec 22, 2021 - Lower riskMedical device
Covidien, LP recalls Palindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 33 cm, Item Code
Covidien recalls specific Palindrome Precision RT Chronic Catheter Kits for updated labeling and instructions to improve safety.
CovidienMay 28, 2021 - Lower riskMedical device
Covidien, LP recalls Adult-Pediatric Electrostatic Filter HME, Item Code 352/5877Z - Product Usage: indicated for single use on anesthetized
Covidien recalls adult-pediatric electrostatic filter HME (item code 352/5877Z) due to potential deviations in ethylene oxide sterilization processes. This product is used for single-use anesthesia and respiratory care. Affected units have specific lot numbers and were sold with certain GTINs.
CovidienApr 29, 2021 - Use cautionMedical device
Covidien, LP recalls Covidien Signia Small Diameter Curved Tip Intelligent Reload 45 mm Vascular/Thin 8 mm - Long Item Code: SIGSDL45CTVT
Covidien recalls specific Signia Small Diameter Curved Tip Intelligent Reload staplers due to potential safety interlock failure, which may cause tissue trauma or bleeding during surgery.
CovidienMar 4, 2021 - Lower riskMedical device
Covidien, LP recalls Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 3.5 mm, Item Code 030452 - Product Usage: The Endo GIA
Covidien recalls Endo GIA Auto Suture Universal Articulating Loading Units with potential incomplete staple formation during surgery, risking bleeding. Affected units have specific lot numbers.
CovidienAug 12, 2020 - Lower riskMedical device
Covidien LP recalls Covidien Vistec" X-Ray Detectable Sponges, 7317 Vistec" X-Ray Detectable Sponges Sponge. product Usage: Vistec X-Ray
Covidien is recalling two lots of X-ray detectable sponges due to possible contamination with human blood during manufacturing. These sponges are used for internal bleeding control and may pose a risk if contaminated.
CovidienJul 17, 2017
Covidien, LP recall questions
How many recalls has Covidien, LP had?
111 recalls from Covidien, LP are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Covidien, LP recall?
Covidien, LP recalls Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31, dated Jun 24, 2026. Every Covidien, LP recall is listed on this page, newest first.
What should I do if I have a recalled Covidien, LP product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Covidien, LP recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.